Variants linked to Height

Continuously updated · newest added Oct 24, 2026

10,054 positions on this site are linked to Height, out of 115,758 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)

DNM3 · rs115924365

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Standard

Height (baseline)

near PRKG2 · rs115355186

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Standard

Height (baseline)

CROCCP3 · rs115126324

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Standard

Height

PENK · rs112083368

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Standard

Height

near LINC02409 · rs11108863

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Standard

Height

near CRB2 · rs10985976

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Standard

Height

TRPM3 · rs10746850

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Standard

Height (baseline)

SFRP4 · rs1052974

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Standard

Height

near GALNT15 · rs9861567

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Standard

Height

TRAK1 · rs9847688

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Standard

Height

REM2 · rs8014119

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Standard

Height (baseline)

near RPS20P10 · rs78479673

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Standard

Height (standard GWA)

LCORL · rs77998009

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Standard

Height (baseline)

CROCC · rs7798

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Standard

Height (baseline)

SLC6A13 · rs77747027

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Standard

Height (baseline)

UBE3D · rs77449736

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Standard

Height (baseline)

IFT140 · rs76393829

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Standard

Height (baseline)

AAK1 · rs76371146

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Standard

Height (standard GWA)

CCDC26 · rs76029466

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Standard

Height (baseline)

IGF2BP1 · rs72833639

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Showing 20 of 10054 · page 91 of 503

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.