Your Analysis

Genetic Predisposition

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

Your Result

Lower Obsessions with washing/cleaning susceptibility predisposition

Was this result accurate for you?

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
58 genes analyzed 0 with detected variants

5S_rRNA 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

5S_rRNA 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

5S_rRNA 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

ANKRD18A GeneCards

ankyrin repeat domain 18A

Genomic Location
Chr 9 Start: 38,571,361 End: 38,620,593 Build: HG19

No SNPs found for this gene in your DNA data.

ATP9A GeneCards

ATPase phospholipid transporting 9A (putative)

Genomic Location
Chr 20 Start: 50,213,053 End: 50,384,929 Build: HG19

No SNPs found for this gene in your DNA data.

BTF3P11 GeneCards

Genomic Location
Chr 13 Start: 77,502,585 End: 77,503,224 Build: HG19

No SNPs found for this gene in your DNA data.

CAMTA1 GeneCards

The protein encoded by this gene contains a CG1 DNA-binding domain, a transcription factor immunoglobulin domain, ankyrin repeats, and calmodulin-binding IQ motifs. The encoded protein is thought to be a transcription factor and may be a tumor suppressor. However, a translocation event is sometimes observed between this gene and the WWTR1 gene, with the resulting WWTR1-CAMTA1 oncoprotein leading to epithelioid hemangioendothelioma, a malignant vascular cancer.

Genomic Location
Chr 1 Start: 6,845,514 End: 7,829,766 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

CHMP2B GeneCards

This gene encodes a component of the heteromeric ESCRT-III complex (Endosomal Sorting Complex Required for Transport III) that functions in the recycling or degradation of cell surface receptors. ESCRT-III functions in the concentration and invagination of ubiquitinated endosomal cargos into intralumenal vesicles. The protein encoded by this gene is found as a monomer in the cytosol or as an oligomer in ESCRT-III complexes on endosomal membranes. It is expressed in neurons of all major regions of the brain. Mutations in this gene result in one form of familial frontotemporal lobar degeneration.

Genomic Location
Chr 3 Start: 87,276,459 End: 87,304,706 Build: HG19

No SNPs found for this gene in your DNA data.

CLN5 GeneCards

This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.

Genomic Location
Chr 13 Start: 77,566,216 End: 77,579,252 Build: HG19

No SNPs found for this gene in your DNA data.

CYLC2 GeneCards

Genomic Location
Chr 9 Start: 105,757,615 End: 105,780,770 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FAM201A GeneCards

Genomic Location
Chr 9 Start: 38,621,085 End: 38,623,281 Build: HG19

No SNPs found for this gene in your DNA data.

FBXL3 GeneCards

F-box and leucine rich repeat protein 3

Genomic Location
Chr 13 Start: 77,579,395 End: 77,601,294 Build: HG19

No SNPs found for this gene in your DNA data.

GBA3 GeneCards

Genomic Location
Chr 4 Start: 22,694,560 End: 22,821,192 Build: HG19

No SNPs found for this gene in your DNA data.

KCTD12 GeneCards

potassium channel tetramerization domain containing 12

Genomic Location
Chr 13 Start: 77,454,310 End: 77,460,540 Build: HG19

No SNPs found for this gene in your DNA data.

LSAMP GeneCards

Genomic Location
Chr 3 Start: 115,521,221 End: 116,164,334 Build: HG19

No SNPs found for this gene in your DNA data.

MIR3194 GeneCards

Genomic Location
Chr 20 Start: 50,069,442 End: 50,069,514 Build: HG19

No SNPs found for this gene in your DNA data.

MIR4795 GeneCards

Genomic Location
Chr 3 Start: 87,275,339 End: 87,275,427 Build: HG19

No SNPs found for this gene in your DNA data.

MYCBP2 GeneCards

This gene encodes an E3 ubiquitin-protein ligase and member of the PHR (Phr1/MYCBP2, highwire and RPM-1) family of proteins. The encoded protein plays a role in axon guidance and synapse formation in the developing nervous system. In mammalian cells, this protein regulates the cAMP and mTOR signaling pathways, and may additionally regulate autophagy. Reduced expression of this gene has been observed in acute lymphoblastic leukemia patients and a mutation in this gene has been identified in patients with a rare inherited vision defect.

Genomic Location
Chr 13 Start: 77,618,792 End: 77,901,229 Build: HG19

No SNPs found for this gene in your DNA data.

NFATC2 GeneCards

nuclear factor of activated T cells 2

Genomic Location
Chr 20 Start: 50,003,500 End: 50,179,378 Build: HG19

No SNPs found for this gene in your DNA data.

POSTN GeneCards

periostin

Genomic Location
Chr 13 Start: 38,136,722 End: 38,172,905 Build: HG19

No SNPs found for this gene in your DNA data.

POU1F1 GeneCards

This gene encodes a member of the POU family of transcription factors that regulate mammalian development. The protein regulates expression of several genes involved in pituitary development and hormone expression. Mutations in this genes result in combined pituitary hormone deficiency. Multiple transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 3 Start: 87,308,554 End: 87,325,734 Build: HG19

No SNPs found for this gene in your DNA data.

SALL4 GeneCards

This gene encodes a zinc finger transcription factor thought to play a role in the development of abducens motor neurons. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS). Alternative splicing results in multiple transcript variants encoding different isoforms.

Genomic Location
Chr 20 Start: 50,398,870 End: 50,419,060 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

TRPC4 GeneCards

This gene encodes a member of the canonical subfamily of transient receptor potential cation channels. The encoded protein forms a non-selective calcium-permeable cation channel that is activated by Gq-coupled receptors and tyrosine kinases, and plays a role in multiple processes including endothelial permeability, vasodilation, neurotransmitter release and cell proliferation. Single nucleotide polymorphisms in this gene may be associated with generalized epilepsy with photosensitivity. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Genomic Location
Chr 13 Start: 38,206,200 End: 38,443,909 Build: HG19

No SNPs found for this gene in your DNA data.

TXNL1 GeneCards

thioredoxin like 1

Genomic Location
Chr 18 Start: 54,264,440 End: 54,305,823 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

U6 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

WDR7 GeneCards

WD repeat domain 7

Genomic Location
Chr 18 Start: 54,318,590 End: 54,697,023 Build: HG19

No SNPs found for this gene in your DNA data.

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Coverage: 2/15 SNPs detected (13%)
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.