Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,639 positions on this site are linked to Height, out of 2,511,617 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

ANTXR1 · rs4241349

See detailed info → Standard

Height

ITPK1 · rs1043542

See detailed info → Standard

Height

near VGLL2 · rs1405212

See detailed info → Standard

Height

TASOR · rs4681725

See detailed info → Standard

Height

near ANAPC13 · rs9841212

See detailed info → Standard

Height

INS-IGF2 · rs4320932

See detailed info → Standard

Height

DIS3L2 · rs3116168

See detailed info → Standard

Height

near SOCS2 · rs11107116

See detailed info → Standard

Height

AFF1 · rs1408

See detailed info → Standard

Height

near LINC02188 · rs10048146

See detailed info → Standard

Height

VGLL4 · rs2276749

See detailed info → Standard

Height

GMPR2 · rs34354104

See detailed info → Standard

Height

SPTY2D1 · rs10832956

See detailed info → Standard

Height

TRIB1AL · rs8180991

See detailed info → Standard

Height (maximum, inv-normal transformed)

MFAP2 · rs55750792

See detailed info → Standard

Height

ACSS2 · rs6088638

See detailed info → Standard

height (mean, inv-normal transformed)

LHPP · rs2362501

See detailed info → Standard

Height

near HMGA1 · rs2780226

See detailed info → Standard

Height

EFEMP1 · rs17278665

See detailed info → Standard

Height

RBL2 · rs17800727

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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.