Variants linked to Height

Continuously updated · newest added Oct 23, 2026

9,584 positions on this site are linked to Height, out of 110,133 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Height

Standard

Height (standard GWA)

COMMD7 · rs13038397

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Standard

Height

near PSMC1P10 · rs12998167

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Standard

Height (standard GWA)

USP10 · rs12932018

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Standard

Height

near MIR148A · rs12700691

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Standard

Height

near FOXO3 · rs1268167

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Standard

Height

near ZIC4 · rs12638416

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Standard

Height

SOX2-OT · rs12635178

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Standard

Height

LINC00607 · rs12623557

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Standard

Height

near 5S_rRNA · rs12532839

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Standard

Height (baseline)

NUSAP1 · rs12148715

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Standard

Height

GABPB2 · rs12090604

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Standard

Height (baseline)

near GIMAP2 · rs118127814

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Standard

Height (baseline)

PPL · rs117818985

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Standard

Height (baseline)

near RNU6-347P · rs117800577

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Standard

Height

RSPO3 · rs11759578

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Standard

Height (baseline)

MAPK9 · rs11744336

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Standard

Height (baseline)

MAX · rs117170128

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Standard

Height (baseline)

MAP3K3 · rs117054431

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Standard

Height

near SH3RF3 · rs11692886

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Standard

Height

near ATP5F1AP2 · rs11683995

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Showing 20 of 9584 · page 40 of 480

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.