Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,227 positions on this site are linked to Height, out of 2,507,279 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

near CASC20 · rs1407039

See detailed info → Standard

Height

PTHLH · rs6252

See detailed info → Standard

Height

MAP2K6 · rs2521348

See detailed info → Standard

Height

ZNF521 · rs4519409

See detailed info → Standard

Height

SYNM-AS1 · rs9672965

See detailed info → Standard

Height

near POLR3A · rs11002344

See detailed info → Standard

Height

near SOST · rs851059

See detailed info → Standard

Standing height (UKB data field 50)

SLFNL1 · rs17357954

See detailed info → Standard

Height

TAF2 · rs10092747

See detailed info → Standard

Height

PHTF2 · rs2428939

See detailed info → Standard

Height

BOC · rs3846046

See detailed info → Standard

Height

near PRDX4P1 · rs963317

See detailed info → Standard

Height

near TET2 · rs10008015

See detailed info → Standard

Height

MECOM · rs7651940

See detailed info → Standard

Height

BRD3 · rs465724

See detailed info → Standard

Height

near KRT18P47 · rs12440803

See detailed info → Standard

Height

DLEU7 · rs2761855

See detailed info → Standard

Height

H6PD · rs2268170

See detailed info → Standard

Height

ESR1 · rs9340955

See detailed info → Standard

Height

SPTBN1 · rs17416284

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Showing 20 of 11227 · page 4 of 562

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.