Variants linked to Height

Continuously updated · newest added Oct 24, 2026

10,038 positions on this site are linked to Height, out of 115,674 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 (baseline)

KDM4B · rs114323300

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Standard

Height (baseline)

IGF1R · rs113868972

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Standard

Height (baseline)

USP37 · rs77149113

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Standard

Height (baseline)

PPP6R3 · rs149002425

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Standard

Height

LINC01562 · rs140830175

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Standard

Height

DET1 · rs13835

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Standard

height (mean, inv-normal transformed)

TENT2 · rs55687040

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Standard

Height

IRS1 · rs4675095

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Standard

Height (baseline)

C3orf70 · rs115926295

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Standard

Height (baseline)

LINC02774 · rs75281702

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Standard

Height

near LINC02751 · rs7128920

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Standard

Height

near ZNF536 · rs6510033

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Standard

Height

CREB3L2 · rs273965

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Standard

Height

TPCN1 · rs2303621

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Standard

Height (baseline)

MLXIP · rs142907186

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Standard

Height (baseline)

near HPDL · rs142895715

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Standard

Height (baseline)

KLHL29 · rs13386930

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Standard

Height (baseline)

CDK12 · rs111458598

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Standard

Height (maximum, inv-normal transformed)

near RNU7-188P · rs971686

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Standard

Height

GRB10 · rs9656664

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Showing 20 of 10038 · page 413 of 502

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.