Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,432 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)

RPS10-NUDT3 · rs540105494

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

PINLYP · rs2682587

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Standing height (UKB data field 50)

MYPN · rs1900016

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Height

near PRKG2 · rs62302280

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Height

HOXD12 · rs847151

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Height

THBS3 · rs35154152

See detailed info → Standard

Height

IGFBP3 · rs6953668

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Height

near FAM76B · rs1255529

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Height

MIR7-3HG · rs3760954

See detailed info → Standard

Height

near LINC01713 · rs6038587

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Height

TAF5 · rs57707166

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Height (baseline)

SLA2 · rs4810266

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height (minimum, inv-normal transformed)

near SSBP3 · rs11206349

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Height (baseline)

DIRC3 · rs74411434

See detailed info → Standard

Height

ADAMTS17 · rs1383543

See detailed info → Standard

Height (baseline)

ZRANB2 · rs66461782

See detailed info → Standard

Height (baseline)

LCORL · rs74537632

See detailed info → Standard

Standing height (UKB data field 50)

near NIP7P1 · rs117327710

See detailed info → Standard

Height

RND3 · rs2222760

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Height

near PDE4B · rs11208844

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Showing 20 of 11114 · page 194 of 556

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.