Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,129 positions on this site are linked to Height, out of 2,506,525 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 KCNH2 · rs2373962

See detailed info → Standard

Height

EPCIP-AS1 · rs4817505

See detailed info → Standard

Height

ESR1 · rs6902771

See detailed info → Standard

Height

SOCS5 · rs3829835

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Height

RREB1 · rs9505086

See detailed info → Standard

Standing height (UKB data field 50)

LINC01526 · rs194619

See detailed info → Standard

Height

SAMD8 · rs11001296

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Height

BMP6 · rs10498672

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Height

CYP26B1 · rs2241057

See detailed info → Standard

Height

near RN7SL865P · rs10219441

See detailed info → Standard

Height (baseline)

BCL2L2-PABPN1 · rs34074573

See detailed info → Standard

height (mean, inv-normal transformed)

ITGB8 · rs17365306

See detailed info → Standard

Height

MFAP2 · rs2284747

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Height

SNHG7 · rs6874

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Height

AP3B1 · rs10514136

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Height

near LINC01960 · rs17308476

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height (minimum, inv-normal transformed)

EPM2A · rs11155426

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Height

TRIM41 · rs17714046

See detailed info → Standard

height (mean, inv-normal transformed)

TLK1 · rs6742854

See detailed info → Standard

height (mean, inv-normal transformed)

HIVEP1 · rs1475356

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Showing 20 of 11129 · page 208 of 557

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.