Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,616 positions on this site are linked to Height, out of 2,511,293 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

Standing height (UKB data field 50)

PITX1-AS1 · rs9327705

See detailed info → Standard

Height (baseline)

near INSYN1-AS1 · rs874956

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Height (baseline)

near SDR16C6P · rs62516734

See detailed info → Standard

Height

SYMPK · rs3745929

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Height

near NPM1P47 · rs17271431

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Height (baseline)

IGF1R · rs149779029

See detailed info → Standard

Height (baseline)

IARS1 · rs78155973

See detailed info → Standard

Height

near MIR17HG · rs7327945

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Height (baseline)

MARS1 · rs7304550

See detailed info → Standard

Height

near RNU2-36P · rs171340

See detailed info → Standard

Height (baseline)

RFC1 · rs12501447

See detailed info → Standard

Standing height (UKB data field 50)

UQCC6 · rs11616083

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Height (baseline)

near INSYN1-AS1 · rs716828

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Height

near LINC01713 · rs6054484

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Height

PARP12 · rs2286198

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Height (baseline)

near RN7SL323P · rs145846214

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Height

PALM2AKAP2 · rs7855586

See detailed info → Standard

Height (baseline)

ARNILA · rs35800274

See detailed info → Standard

Height (standard GWA)

ADAMTS19 · rs1363146

See detailed info → Standard

Standing height (UKB data field 50)

near LINC01635 · rs12730256

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Showing 20 of 11616 · page 578 of 581

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.