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All variants

Continuously updated · newest added Nov 6, 2026

2,500,918 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

Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs1557229683

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs2148329890

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs200111236

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Standard

G6PD SANTIAGO

G6PD · rs137852332

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Standard

G6PD JAPAN

G6PD · rs137852336

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs2070346788

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Standard

G6PD LOMA LINDA

G6PD · rs137852329

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Standard

G6PD AVEIRO

G6PD · rs137852346

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs2148330566

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs2148328852

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Sensitive

Inborn genetic diseases

G6PD · rs1557229736

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs2148328873

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Standard

G6PD SANTIAGO DE CUBA

G6PD · rs137852317

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Standard

G6PD ANDALUS

G6PD · rs137852324

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Standard

G6PD TOMAH

G6PD · rs137852322

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs1603411177

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Standard

G6PD PUERTO LIMON

G6PD · rs387906468

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Standard

G6PD NANKANG

G6PD · rs137852343

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs2523261737

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Standard

Anemia, nonspherocytic hemolytic, due to G6PD deficiency

G6PD · rs1557229599

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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.