All variants

Continuously updated · newest added Sep 14, 2026

9,513 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 on its own

Electroencephalographic traits in alcoholism

KCNJ6 · rs2835872

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Standard

Cholesterol, total

TRPS1 · rs2737229

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Sensitive

Rheumatoid arthritis

TEC · rs2664035

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Sensitive

Rheumatoid arthritis

TNFAIP3 · rs7752903

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Sensitive

Response to thiopurine immunosuppressants in inflammatory bowel disease (pancreatitis) (azathioprine and mercaptopurine)

HLA region · rs6935723

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Standard

Educational attainment

POU3F2 · rs1487441

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Standard

Educational attainment

RNF123 · rs9858213

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Standard

Vitamin D levels

PDE3B · rs11023332

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Standard

Vitamin D levels

CYP2R1 · rs1007392

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Standard

Educational attainment

ASB18 · rs13401104

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Standard

Educational attainment

LRRN2 · rs3789044

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Standard

Vitamin D levels

GC · rs17467825

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Standard on its own

Osteoprotegerin levels

MIR4723 · rs704

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Standard on its own

Osteoprotegerin levels

COLEC10 · rs1425053

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Standard on its own

Superior frontal gyrus grey matter volume

EIF4G3 · rs4654899

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Standard

Hypospadias

DGKK · rs4554617

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Sensitive

Response to radiotherapy in prostate cancer (toxicity)

TANC1 · rs7582141

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Standard

Cholesterol, total

CETP · rs118146573

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Standard

HDL cholesterol

SIK3 · rs11216230

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Standard

Hypospadias

TAX1BP1 · rs10214930

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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.