Genetic Predisposition

Based on your genetic markers, your predisposition to this trait is shown below

Your Result

Average genetic predisposition

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Scientific Evidence

Understanding the Data
  • SNP: A specific genetic marker relevant to this trait (e.g., rs2588978)
  • Genotype: Your genetic makeup at the given SNP location (e.g., CC)
  • Variant allele: The alternative DNA sequence at the SNP site
  • Variant allele frequency: Percentage of population carrying this variant
  • Variant found: Whether the variant was detected in your DNA file
36 genes analyzed 5 with detected variants
Variant Detected

ATF6B GeneCards

The protein encoded by this gene is a transcription factor in the unfolded protein response (UPR) pathway during ER stress. Either as a homodimer or as a heterodimer with ATF6-alpha, the encoded protein binds to the ER stress response element, interacting with nuclear transcription factor Y to activate UPR target genes. The protein is normally found in the membrane of the endoplasmic reticulum

Genomic Location
Chr 6 Start: 32,083,041 End: 32,096,023 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

CADM2 GeneCards

cell adhesion molecule 2

Genomic Location
Chr 3 Start: 85,008,140 End: 86,123,579 Build: HG19
Associated SNPs
1 / 3 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

GOT2 GeneCards

glutamic-oxaloacetic transaminase 2

Genomic Location
Chr 16 Start: 58,741,035 End: 58,768,220 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

HLA-DQB1 GeneCards

Genomic Location
Chr 6 Start: 32,627,244 End: 32,634,434 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected
Genomic Location
Chr 6 Start: 97,590,037 End: 97,731,092 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ARC GeneCards

activity regulated cytoskeleton associated protein

Genomic Location
Chr 8 Start: 143,692,410 End: 143,695,840 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ARID5B GeneCards

This gene encodes a member of the AT-rich interaction domain (ARID) family of DNA binding proteins. The encoded protein forms a histone H3K9Me2 demethylase complex with PHD finger protein 2 and regulates the transcription of target genes involved in adipogenesis and liver development. This gene also plays a role in cell growth and differentiation of B-lymphocyte progenitors, and single nucleotide polymorphisms in this gene are associated with acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Genomic Location
Chr 10 Start: 63,661,458 End: 63,856,703 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ARPC3 GeneCards

actin related protein 2/3 complex subunit 3

Genomic Location
Chr 12 Start: 110,872,628 End: 110,888,142 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ATP2B1 GeneCards

The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 1. Alternatively spliced transcript variants encoding different isoforms have been identified. COMPLETENESS: complete on the 3' end.

Genomic Location
Chr 12 Start: 89,981,826 End: 90,103,143 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

BHLHE22 GeneCards

This gene encodes a protein that belongs to the basic helix-loop-helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis.

Genomic Location
Chr 8 Start: 65,492,922 End: 65,496,184 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CD34 GeneCards

CD34 molecule

Genomic Location
Chr 1 Start: 208,054,317 End: 208,084,470 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CDH8 GeneCards

cadherin 8

Genomic Location
Chr 16 Start: 61,681,154 End: 62,070,342 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CDSN GeneCards

corneodesmosin

Genomic Location
Chr 6 Start: 31,082,864 End: 31,088,223 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CTIF GeneCards

cap binding complex dependent translation initiation factor

Genomic Location
Chr 18 Start: 46,065,402 End: 46,389,588 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 12 Start: 22,778,105 End: 22,843,599 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FOXP1 GeneCards

This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms. COMPLETENESS: complete on the 3' end.

Genomic Location
Chr 3 Start: 71,003,859 End: 71,633,129 Build: HG19
Associated SNPs
0 / 2 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

GADD45G GeneCards

Genomic Location
Chr 9 Start: 92,219,927 End: 92,221,470 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 17 Start: 47,035,916 End: 47,045,958 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 3 Start: 52,719,936 End: 52,728,513 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

HLA-DRB5 GeneCards

major histocompatibility complex, class II, DR beta 5

Genomic Location
Chr 6 Start: 32,485,130 End: 32,498,064 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 6 Start: 19,837,601 End: 19,842,428 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ISL1 GeneCards

This gene encodes a member of the LIM/homeodomain family of transcription factors. The encoded protein binds to the enhancer region of the insulin gene, among others, and may play an important role in regulating insulin gene expression. The encoded protein is central to the development of pancreatic cell lineages and may also be required for motor neuron generation. Mutations in this gene have been associated with maturity-onset diabetes of the young.

Genomic Location
Chr 5 Start: 50,679,282 End: 50,690,564 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

KANSL1 GeneCards

This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The corresponding protein in Drosophila interacts with K(lysine) acetyltransferase 8, which is also a subunit of both the MLL1 and NSL1 complexes.

Genomic Location
Chr 17 Start: 44,107,282 End: 44,302,733 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

KCNJ3 GeneCards

potassium inwardly rectifying channel subfamily J member 3

Genomic Location
Chr 2 Start: 155,555,207 End: 155,714,866 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

KCNJ4 GeneCards

Several different potassium channels are known to be involved with electrical signaling in the nervous system. One class is activated by depolarization whereas a second class is not. The latter are referred to as inwardly rectifying K+ channels, and they have a greater tendency to allow potassium to flow into the cell rather than out of it. This asymmetry in potassium ion conductance plays a key role in the excitability of muscle cells and neurons. The protein encoded by this gene is an integral membrane protein and member of the inward rectifier potassium channel family. The encoded protein has a small unitary conductance compared to other members of this protein family. Two transcript variants encoding the same protein have been found for this gene.

Genomic Location
Chr 22 Start: 38,822,332 End: 38,851,205 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 11 Start: 30,405,626 End: 30,607,900 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MSANTD1 GeneCards

Genomic Location
Chr 4 Start: 3,246,096 End: 3,258,340 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 19 Start: 3,359,628 End: 3,469,215 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

NOA1 GeneCards

nitric oxide associated 1

Genomic Location
Chr 4 Start: 57,829,516 End: 57,843,772 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

PAPPA2 GeneCards

This gene encodes a member of the pappalysin family of metzincin metalloproteinases. The encoded protein cleaves insulin-like growth factor-binding protein 5 and is thought to be a local regulator of insulin-like growth factor (IGF) bioavailability. Alternative splicing results in multiple transcript variants.

Genomic Location
Chr 1 Start: 176,432,311 End: 176,814,737 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SGIP1 GeneCards

SH3GL interacting endocytic adaptor 1

Genomic Location
Chr 1 Start: 66,999,044 End: 67,216,822 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SOX11 GeneCards

This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The protein may function in the developing nervous system and play a role in tumorigenesis.

Genomic Location
Chr 2 Start: 5,832,516 End: 5,841,517 Build: HG19
Associated SNPs
0 / 2 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

TCF4 GeneCards

This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described.

Genomic Location
Chr 18 Start: 52,889,416 End: 53,303,188 Build: HG19
Associated SNPs
0 / 2 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

TNXB GeneCards

This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 6 Start: 32,008,930 End: 32,077,115 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

TTBK1 GeneCards

tau tubulin kinase 1

Genomic Location
Chr 6 Start: 43,211,219 End: 43,255,996 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Genomic Location
Chr 8 Start: 10,753,555 End: 11,059,342 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

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Coverage: 5/42 SNPs detected (11%)
Reference: Human Genome Build 37 (HG19)
Generated: March 02, 2026
DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence. Other testing companies may report using the opposite strand, requiring conversion for accurate comparison.