Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,771 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

AUTS2 · rs79048874

See detailed info → Standard

Height (baseline)

FAM240A · rs79036361

See detailed info → Standard

Height (baseline)

near TRPS1 · rs78524196

See detailed info → Standard

Height

TG · rs7844761

See detailed info → Standard

Height (baseline)

near NACA2 · rs77893494

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Height (baseline)

TRPS1 · rs77193180

See detailed info → Standard

Height

near AMD1P1 · rs77164188

See detailed info → Standard

Height (baseline)

FST · rs76803798

See detailed info → Standard

Height (baseline)

PDK4-AS1 · rs76276659

See detailed info → Standard

Height (baseline)

NAV3 · rs76219170

See detailed info → Standard

Height (baseline)

AGAP1 · rs7590181

See detailed info → Standard

Height

near LINC01751 · rs75479361

See detailed info → Standard

Height

SPACA6 · rs75253143

See detailed info → Standard

Height (baseline)

FBXW11 · rs75245326

See detailed info → Standard

Height (standard GWA)

PREX1 · rs75223094

See detailed info → Standard

Height (baseline)

near LINC02636 · rs75130818

See detailed info → Standard

Height (standard GWA)

IGF2BP2 · rs73175571

See detailed info → Standard

Height (baseline)

LRP8 · rs72895378

See detailed info → Standard

Height (baseline)

USP8 · rs72738959

See detailed info → Standard

Height (baseline)

GUSBP5 · rs72729595

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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.