Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,015 positions on this site are linked to Height, out of 2,506,010 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

DIRC3 · rs11686077

See detailed info → Standard

Height

PRRC2A · rs2242657

See detailed info → Standard

Height

MLLT1 · rs12979828

See detailed info → Standard

Height

near FLNB · rs11130605

See detailed info → Standard

Height

GCOM1 · rs1062707

See detailed info → Standard

Height

NOTCH4 · rs8192565

See detailed info → Standard

Height

HMGN2 · rs6703872

See detailed info → Standard

Height

near ERP27 · rs2430691

See detailed info → Standard

Height

near MIX23P2 · rs7096841

See detailed info → Standard

Height

LINC01524 · rs6021801

See detailed info → Standard

Height

FKBP14-AS1 · rs2302626

See detailed info → Standard

Height

SYNE1 · rs2813501

See detailed info → Standard

Height

SSTR5-AS1 · rs213658

See detailed info → Standard

Height

near EXOC7P1 · rs1452404

See detailed info → Standard

Height

ERBB4 · rs13389790

See detailed info → Standard

Height

near LINC02872 · rs10746796

See detailed info → Standard

Height

AKT1 · rs10142069

See detailed info → Standard

Height

KIAA1191P3 · rs6700582

See detailed info → Standard

Height

ACOXL · rs2341897

See detailed info → Standard

Height

ZNF628 · rs2059137

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Showing 20 of 11015 · page 168 of 551

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.