Your Analysis

Genetic Predisposition

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

Your Result

Higher Bunions susceptibility 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
53 genes analyzed 2 with detected variants
Variant Detected

CMTM7 GeneCards

Genomic Location
Chr 3 Start: 32,433,345 End: 32,497,020 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

PPP4R1L GeneCards

Genomic Location
Chr 20 Start: 56,807,833 End: 56,884,495 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

AC007682.1 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 2 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

AC019330.1 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ACTG1P9 GeneCards

Genomic Location
Chr 6 Start: 46,172,649 End: 46,174,298 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ANKFN1 GeneCards

Genomic Location
Chr 17 Start: 54,230,836 End: 54,594,377 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ARHGEF1 GeneCards

Rho guanine nucleotide exchange factor 1

Genomic Location
Chr 19 Start: 42,387,251 End: 42,411,604 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CLCA2 GeneCards

chloride channel accessory 2

Genomic Location
Chr 1 Start: 86,889,854 End: 86,922,236 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

COL24A1 GeneCards

This gene is a member of the collagen gene family and is thought to regulate type I collagen fibrillogenesis during fetal development.

Genomic Location
Chr 1 Start: 86,194,916 End: 86,622,667 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

DPYS GeneCards

Dihydropyrimidinase catalyzes the conversion of 5,6-dihydrouracil to 3-ureidopropionate in pyrimidine metabolism. Dihydropyrimidinase is expressed at a high level in liver and kidney as a major 2.5-kb transcript and a minor 3.8-kb transcript. Defects in the DPYS gene are linked to dihydropyrimidinuria.

Genomic Location
Chr 8 Start: 105,391,659 End: 105,479,283 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

DSCAM GeneCards

DS cell adhesion molecule

Genomic Location
Chr 21 Start: 41,382,926 End: 42,219,084 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

DSN1 GeneCards

DSN1 component of MIS12 kinetochore complex

Genomic Location
Chr 20 Start: 35,380,198 End: 35,402,166 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

EYS GeneCards

The product of this gene contains multiple epidermal growth factor (EGF)-like and LamG domains. The protein is expressed in the photoreceptor layer of the retina, and the gene is mutated in autosomal recessive retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 6 Start: 64,429,876 End: 66,417,119 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

GRIN2A GeneCards

This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants.

Genomic Location
Chr 16 Start: 9,847,261 End: 10,276,765 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

L3MBTL4 GeneCards

Genomic Location
Chr 18 Start: 5,954,716 End: 6,415,258 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LINC00448 GeneCards

Genomic Location
Chr 13 Start: 63,246,418 End: 63,381,492 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LINC00540 GeneCards

Genomic Location
Chr 13 Start: 22,784,424 End: 22,850,660 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LINC02074 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LUZP2 GeneCards

Genomic Location
Chr 11 Start: 24,518,599 End: 25,104,184 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MTR GeneCards

This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

Genomic Location
Chr 1 Start: 236,958,581 End: 237,067,281 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MYO1B GeneCards

myosin IB

Genomic Location
Chr 2 Start: 192,110,130 End: 192,290,112 Build: HG19
Associated SNPs
0 / 2 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ODF2L GeneCards

outer dense fiber of sperm tails 2 like

Genomic Location
Chr 1 Start: 86,812,520 End: 86,862,006 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

OPCML GeneCards

This gene encodes a member of the IgLON subfamily in the immunoglobulin protein superfamily of proteins. The encoded preprotein is proteolytically processed to generate the mature protein. This protein is localized in the plasma membrane and may have an accessory role in opioid receptor function. This gene has an ortholog in rat and bovine. The opioid binding-cell adhesion molecule encoded by the rat gene binds opioid alkaloids in the presence of acidic lipids, exhibits selectivity for mu ligands and acts as a GPI-anchored protein. Since the encoded protein is highly conserved in species during evolution, it may have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.

Genomic Location
Chr 11 Start: 132,284,559 End: 133,402,396 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

RFLNA GeneCards

Genomic Location
Chr 12 Start: 124,773,710 End: 124,800,570 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

RFLNA GeneCards

Genomic Location
Chr 12 Start: 124,457,762 End: 124,800,570 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

RNU6-1213P GeneCards

Genomic Location
Chr 8 Start: 81,317,751 End: 81,317,844 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SLC8A1-AS1 GeneCards

SLC8A1 antisense RNA 1

Genomic Location
Chr 2 Start: 40,144,774 End: 40,482,349 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SLIT3 GeneCards

The protein encoded by this gene is secreted, likely interacting with roundabout homolog receptors to effect cell migration. Two transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 5 Start: 168,088,745 End: 168,728,143 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SOX2-OT GeneCards

SOX2 overlapping transcript

Genomic Location
Chr 3 Start: 180,774,468 End: 181,460,016 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U8 GeneCards

Genomic Location
Chr ? Start: N/A End: N/A Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

WASF3 GeneCards

WASP family member 3

Genomic Location
Chr 13 Start: 27,131,820 End: 27,263,085 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

WDR27 GeneCards

This gene encodes a protein with multiple WD repeats. Proteins with these repeats may form scaffolds for protein-protein interaction and play key roles in cell signalling. Alternative splicing results in multiple transcript variants, but the full-length structure of some of these variants cannot be determined.

Genomic Location
Chr 6 Start: 169,857,307 End: 170,102,125 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
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Coverage: 2/44 SNPs detected (4%)
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.