Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,479 positions on this site are linked to Height, out of 2,509,486 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 HMGN1P19 · rs62452707

See detailed info → Standard

Height

EYA4 · rs62430323

See detailed info → Standard

Height (baseline)

near RPSAP72 · rs62424471

See detailed info → Standard

Height (baseline)

near TTK · rs62405996

See detailed info → Standard

Height (standard GWA)

DMP1-AS1 · rs62315988

See detailed info → Standard

Height (baseline)

KCNJ16 · rs62081370

See detailed info → Standard

Height (baseline)

near RNU4-10P · rs61966318

See detailed info → Standard

Height

SLC13A3 · rs6122514

See detailed info → Standard

Height (baseline)

ASTN2 · rs60477877

See detailed info → Standard

Height (baseline)

PGA5 · rs603061

See detailed info → Standard

Height (baseline)

DNM3 · rs59396474

See detailed info → Standard

Height

near DERL3 · rs5751749

See detailed info → Standard

Height (baseline)

MFSD14B · rs569900068

See detailed info → Standard

Height (baseline)

PPP4R4 · rs569713795

See detailed info → Standard

Height

near RPL31P32 · rs566773279

See detailed info → Standard

Height (baseline)

CENPP · rs564507908

See detailed info → Standard

Height (baseline)

CCDC144BP · rs562273821

See detailed info → Standard

Height (baseline)

ANKS1A · rs561189520

See detailed info → Standard

Height (baseline)

ANTXR1 · rs56094178

See detailed info → Standard

Height (baseline)

near PCAT7 · rs55785529

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Showing 20 of 11479 · page 270 of 574

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.