All variants

Continuously updated · newest added Sep 12, 2026

7,216 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

Atrial fibrillation/atrial flutter

PITX2 · rs10033464

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Standard on its own

Response to bleomycin (chromatid breaks)

PMAIP · rs8093763

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Standard

Obesity-related traits

FTO · rs9930506

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Standard

Ulcerative colitis

IL17REL · rs5771069

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Sensitive

Inflammatory bowel disease

TNFRSF6B · rs2315008

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Sensitive

Restless legs syndrome

MEIS1 · rs2300478

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Standard

Folate metabolism (MTHFR A1298C)

MTHFR · rs1801131

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Standard

Vitamin D levels

GC · rs2282679

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Standard

Freckling & sun sensitivity

IRF4 · rs12203592

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Standard

Triglyceride levels

APOA5 · rs662799

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Standard on its own

Hair thickness

EDAR · rs3827760

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Sensitive

Iron overload risk (HFE H63D)

HFE · rs1799945

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Standard

Height

PLAG1 · rs13273123

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Standard

Carotenoid and tocopherol levels

APOA5 · rs12272004

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Standard

Height

HMGA1 · rs6918981

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Sensitive

Warfarin sensitivity

VKORC1 · rs9923231

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Sensitive

Iron overload risk (hereditary hemochromatosis)

HFE · rs1800562

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Standard

Male pattern baldness tendency

AR · rs6152

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Standard

ABO blood type

ABO · rs8176719

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Standard

Duffy blood group (malaria resistance)

DARC / ACKR1 · rs2814778

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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.