All variants

Continuously updated · newest added Oct 21, 2026

103,190 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

Educational attainment

NOS1AP · rs80159981

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Mean platelet volume during third trimester of pregnancy

NOS1AP · rs78344479

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Standard

Smoking cessation

NOS1AP · rs4657158

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Standard

Smoking cessation

NOS1AP · rs10918790

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Standard

Platelet count

NOS1AP · rs6684278

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Standard

Mean reticulocyte volume (UKB data field 30260)

NOS1AP · rs7536043

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Standard

FCGR2A protein levels

NOS1AP · rs146009967

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Standard

FCGR2A protein levels

NOS1AP · rs560123160

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FCGR3B protein levels

NOS1AP · rs114836703

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Standard

monocyte (fraction, minimum, inv-norm transformed)

NOS1AP · rs10918705

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Standard on its own

FCRLB protein levels

near NOS1AP · rs12136975

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Standard

Low affinity immunoglobulin gamma Fc region receptor II-b levels

NOS1AP · rs189676321

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Standard

FCGR2A protein levels

NOS1AP · rs7539084

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Standard

FCRLB protein levels

NOS1AP · rs191648462

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Standard

FCGR3B protein levels

NOS1AP · rs10800384

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Standard

Monocyte count

NOS1AP · rs60441301

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Monocyte percentage of white cells

NOS1AP · rs6677530

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Granulocyte percentage of myeloid white cells

NOS1AP · rs6658646

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Body mass index (change over time)

NOS1AP · rs347313

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Standard

QT interval

NOS1AP · rs347272

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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.