Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

All variants

Continuously updated · newest added Nov 7, 2026

2,504,943 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.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

Sensitive

Gilbert syndrome

UGT1A1 · rs4148324

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Sensitive

Crigler-Najjar syndrome

UGT1A1 · rs1042640

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Standard

Hyperbilirubinemia

UGT1A1 · rs587784535

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Sensitive

Gilbert syndrome

UGT1A1 · rs1373930486

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Sensitive

Gilbert syndrome

UGT1A1 · rs2126038220

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Sensitive

Crigler-Najjar syndrome type 1

UGT1A1 · rs587776764

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Sensitive

Crigler-Najjar syndrome

UGT1A1 · rs367897068

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Sensitive

Crigler-Najjar syndrome type 1

UGT1A1 · rs72551349

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Sensitive

UGT1A1-related disorder

UGT1A1 · rs1476500325

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Standard

BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1

UGT1A1 · rs1424603943

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Sensitive

Crigler-Najjar syndrome

UGT1A1 · rs72551340

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Sensitive

Crigler-Najjar syndrome

UGT1A1 · rs139607673

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Sensitive

Crigler-Najjar syndrome

UGT1A1 · rs72551343

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Sensitive

Crigler-Najjar syndrome type 1

UGT1A1 · rs72551353

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Sensitive

UGT1A1-related disorder

UGT1A1 · rs72551350

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Sensitive

Gilbert syndrome

UGT1A1 · rs56059937

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Sensitive

Lucey-Driscoll syndrome

UGT1A1 · rs34993780

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Sensitive

Crigler-Najjar syndrome type 1

UGT1A1 · rs62625011

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Standard

Total bilirubin levels (UKB data field 30840)

near UGT1A11P · rs184026545

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Standard

Total bilirubin levels (UKB data field 30840)

UGT1A10 · rs138562568

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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.