Gene Knowledge Graph
UTC

All variants

Continuously updated · newest added Oct 22, 2026

107,852 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.

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DNA-incorporated thioguanine levels in 6-mercaptopurine-treated acute lymphoblastic leukaemia

TPMT · rs79050301

See detailed info → Standard

TPMT protein levels

RNF144B · rs10949517

See detailed info → Standard

TPMT protein levels

near ID4 · rs192843721

See detailed info → Standard

TPMT protein levels

KIF13A · rs562345710

See detailed info → Standard

TPMT protein levels

near RPL21P61 · rs72830515

See detailed info → Standard

TPMT protein levels

near RNF144B · rs190235604

See detailed info → Standard

TPMT protein levels

TPMT · rs138317895

See detailed info → Standard

TPMT protein levels

TPMT · rs1800462

See detailed info → Standard

TPMT protein levels

KDM1B · rs187686404

See detailed info → Standard

Thiopurine S-methyltransferase activity

TPMT · rs73726531

See detailed info → Standard

TPMT protein levels

KDM1B · rs551155433

See detailed info → Standard

Intrinsic epigenetic age acceleration

TPMT · rs76244256

See detailed info → Standard

Erythrocyte methylated 6-mercaptopurine metabolite concentration in 6-mercaptopurine-treated acute lymphoblastic leukaemia

TPMT · rs10949482

See detailed info → Sensitive

TPMT *3C — thiopurine tolerance

TPMT · rs1142345

See detailed info → Sensitive

NUDT15 *3 — thiopurine tolerance

NUDT15 · rs116855232

See detailed info →

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.