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

RERE · rs11586056

See detailed info → Standard

Height

HIVEP1 · rs4714150

See detailed info → Standard

Height

EPB41L4B · rs10979739

See detailed info → Standard

Height

near H1-0 · rs4821714

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Height (baseline)

DOCK3 · rs141494203

See detailed info → Standard

Height

ADPGK · rs12908694

See detailed info → Standard

Height

EPB41L2 · rs12965

See detailed info → Standard

Height

near SMCO4P1 · rs8072790

See detailed info → Standard

Height

GCAT · rs2285179

See detailed info → Standard

Height

NDUFAF7 · rs12622740

See detailed info → Standard

Height

RORA-AS1 · rs17191442

See detailed info → Standard

Height

RALY · rs17091470

See detailed info → Standard

Height

KIF7 · rs11630411

See detailed info → Standard

Height

ELP1 · rs10979605

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Height

near DIDO1 · rs1077418

See detailed info → Standard

Height

near SLC25A37 · rs41460846

See detailed info → Standard

Height

near C14orf39 · rs17256101

See detailed info → Standard

Height

SOCS2-AS1 · rs10859518

See detailed info → Standard

Height

PRDM11 · rs3758726

See detailed info → Standard

Height

CCND2 · rs3217862

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Showing 20 of 11659 · page 41 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.