Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,659 positions on this site are linked to Height, out of 2,511,894 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

HS6ST3 · rs626317

See detailed info → Standard

Height (baseline)

near GHSR · rs519384

See detailed info → Standard

Height

GPNMB · rs13240597

See detailed info → Standard

Height

ASTN1 · rs12747720

See detailed info → Standard

Height

TGFBR1 · rs868

See detailed info → Standard

Height

NFATC1 · rs3786204

See detailed info → Standard

Height

near RNU6-92P · rs6947682

See detailed info → Standard

Height

CRADD · rs17732565

See detailed info → Standard

Height

SAMD12 · rs12680308

See detailed info → Standard

Height

near TMED7 · rs13160138

See detailed info → Standard

Height

PITPNM1 · rs11604662

See detailed info → Standard

Height

CASP16P · rs2550392

See detailed info → Standard

Height

near CYS1 · rs12990115

See detailed info → Standard

Height

EP400P1 · rs12303540

See detailed info → Standard

Height

MAP4K5 · rs12050306

See detailed info → Standard

Height

LINC02694 · rs10520107

See detailed info → Standard

Height

COL14A1 · rs7819160

See detailed info → Standard

Height

near NEK7 · rs2359675

See detailed info → Standard

Height

PGS1 · rs2292641

See detailed info → Standard

Height

near CYP26B1 · rs7575536

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Showing 20 of 11659 · page 39 of 583

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.