All variants

Continuously updated · newest added Sep 13, 2026

7,939 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

Urate levels

near ZNF518B · rs79824542

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Sensitive

Breast cancer

PTHLH · rs10771399

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Standard

Urate levels

ZNF518B · rs34208161

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Standard on its own

Circulating myeloperoxidase levels (plasma)

C17orf71 · rs6503905

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Standard on its own

Circulating myeloperoxidase levels (plasma)

MPO · rs12940923

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Standard

Urate levels

SLC2A9 · rs80204783

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Standard

Urate levels

SLC2A9 · rs116142041

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Standard

Chronic lymphocytic leukemia

ACOXL · rs17483466

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Standard

Chronic lymphocytic leukemia

MNS1 · rs11636802

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Sensitive

End-stage renal disease in Type 1 diabetics

CDCA7 · rs4972593

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Standard

Body mass index and fasting glucose (pairwise)

ADCY9 · rs879620

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Standard

Body mass index and fasting glucose (pairwise)

PCSK1 · rs7713317

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Standard on its own

Body mass index and fasting glucose (pairwise)

ADCY5 · rs11708067

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Standard

Body mass index and triglycerides (pairwise)

SLC22A3 · rs539958

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Standard

Body mass index and triglycerides (pairwise)

STK36 · rs1427445

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Standard

Body mass index and HDL-C (pairwise)

CCDC92-DNAH10 · rs7133378

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Standard

Body mass index and HDL-C (pairwise)

INHBC · rs3741414

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Standard

Body mass index and HDL-C (pairwise)

ARL15 · rs3776717

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Standard

Body mass index and HDL-C (pairwise)

ETV5 · rs4234589

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Standard on its own

Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test)

SLC30A10 · rs2820443

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Showing 20 of 7939 · page 289 of 397

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.