All variants

Continuously updated · newest added Sep 13, 2026

7,772 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.

Standard

C-reactive protein levels

HNF4A · rs1800961

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Standard

C-reactive protein levels

SALL1 · rs10521222

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Standard on its own

N-glycan levels

NRTN · rs3760776

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Standard

Height

GPR126 · rs4896582

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Standard

Mean corpuscular volume

CD164 · rs9374080

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Standard

Mean corpuscular volume

MARCH8 · rs11239550

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Sensitive

Parkinson's disease

MAPT · rs393152

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Standard

Mean corpuscular volume

RTBDN · rs7255045

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Standard on its own

Soluble levels of adhesion molecules

ICAM-1 · rs3093030

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Standard

Pulmonary function

THSD4 · rs12899618

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Standard on its own

Adiponectin levels

ADIPOQ · rs1648707

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Standard

Mean corpuscular hemoglobin

GCDH · rs11085824

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Standard

C-reactive protein

IL6 · rs2097677

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Sensitive

Polycystic ovary syndrome

ZFP36L2 · rs13429458

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Sensitive

Polycystic ovary syndrome

DENND1A · rs10818854

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Sensitive

Prostate cancer

near SMIM38 · rs7931342

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Standard

Age-related macular degeneration

CFB · rs9380272

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Standard on its own

Diabetic retinopathy

near PLXDC2 · rs12219125

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Standard

Primary tooth development (number of teeth)

KCNJ2 · rs8079702

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Standard on its own

Bone mineral density (hip)

ARHGAP1 · rs7932354

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.