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 2,511,952 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

SLIT3 · rs2938763

See detailed info → Standard

Height

CNGB3 · rs2304790

See detailed info → Standard

Height

ATP2B1-AS1 · rs17783015

See detailed info → Standard

Height

CASC9 · rs16939034

See detailed info → Standard

Height

FAM234B · rs950671

See detailed info → Standard

Height

NR3C1 · rs852982

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Height

near CHSY1 · rs2170625

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Height

near CRADD · rs7963343

See detailed info → Standard

Height (baseline)

DNM3 · rs61807763

See detailed info → Standard

Height

MAP2K2 · rs350897

See detailed info → Standard

Height

TET1 · rs2795870

See detailed info → Standard

Height

LINC01107 · rs11888775

See detailed info → Standard

Height

near E2F7 · rs12831350

See detailed info → Standard

Height

IGF2BP2 · rs7634540

See detailed info → Standard

Height

COMMD4 · rs11853141

See detailed info → Standard

Height

PSME4 · rs805415

See detailed info → Standard

Height

KAT2A · rs730086

See detailed info → Standard

Height

BRAF · rs2364399

See detailed info → Standard

Height

near CCDC194 · rs17457472

See detailed info → Standard

Height

near WNT4 · rs12734979

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Showing 20 of 11659 · page 43 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.