All variants

Continuously updated · newest added Sep 12, 2026

7,519 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

Cholesterol, total

ASAP3 · rs1077514

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Sensitive

Polycystic ovary syndrome

SUMO1P1 · rs6022786

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Sensitive

Polycystic ovary syndrome

HMGA2 · rs2272046

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Sensitive

Polycystic ovary syndrome

YAP1 · rs1894116

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Sensitive

Polycystic ovary syndrome

C9orf3 · rs3802457

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Sensitive

Schizophrenia

HHAT · rs7527939

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Sensitive

Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma)

SP4 · rs2285947

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Sensitive

Prostate cancer

near POU5F1B · rs10505483

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Sensitive

Prostate cancer

near POU5F1B · rs6983561

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Standard on its own

Coffee consumption (cups per day)

MLXIPL · rs7800944

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Standard on its own

Coffee consumption (cups per day)

EFCAB5 · rs9902453

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Standard on its own

Vertical cup-disc ratio

DUSP1 · rs17658229

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Sensitive

Alzheimer's disease (late onset)

SLC24A4 · rs10498633

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Standard on its own

Liver enzyme levels (gamma-glutamyl transferase)

ITGA1 · rs4074793

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Standard on its own

Fractional exhaled nitric oxide (childhood)

LYRM9 · rs3751972

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Standard

Plasma plasminogen activator levels

STXBP5 · rs9399599

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Standard on its own

Urinary uromodulin levels

PDILT · rs12446492

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Standard on its own

Pulmonary emphysema

MAN2B1 · rs10411619

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Sensitive

Breast cancer

CDYL2 · rs13329835

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Sensitive

Breast cancer

COX11 · rs6504950

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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.