Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,272 positions on this site are linked to Height, out of 2,507,630 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

CDC42EP3-AS1 · rs17021261

See detailed info → Standard

Height

HIPK2 · rs11770283

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Height

near RPL37P6 · rs11990963

See detailed info → Standard

Height

near NUP37 · rs11111147

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Standing height (UKB data field 50)

NCOR2 · rs10846657

See detailed info → Standard

Height

MAP7D1 · rs4653164

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Height

near BMP2 · rs6085728

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Height

near CCNE1 · rs4556910

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Height

near EVX1-AS · rs12700794

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Height

near SH3D21 · rs4653178

See detailed info → Standard

Height

CRISPLD2 · rs1466716

See detailed info → Standard

Height

ADAMTSL1 · rs1412673

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Height

near RNU6-1328P · rs12704720

See detailed info → Standard

Height

LINC02997 · rs4976023

See detailed info → Standard

Height

WWOX · rs4502225

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Height

near LINC00607 · rs10932618

See detailed info → Standard

Height

CDC42EP3-AS1 · rs12615742

See detailed info → Standard

Height

SIM2 · rs737380

See detailed info → Standard

Height

near BMP2 · rs6054512

See detailed info → Standard

Height

LINC02725 · rs10893818

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Showing 20 of 11272 · page 563 of 564

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.