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

E2F7 · rs7976940

See detailed info → Standard

Height (baseline)

RCBTB1 · rs193054544

See detailed info → Standard

Height

BCL11A · rs10184550

See detailed info → Standard

Height

COPB1 · rs79732015

See detailed info → Standard

Height

ZFAT · rs4909912

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Height

near Y_RNA · rs16823787

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Height

near TTC4P1 · rs1540824

See detailed info → Standard

Height

ESR1 · rs3798758

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Height

NSF · rs35937770

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Height

ARID4A · rs10137475

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Height

near CYP26B1 · rs4852850

See detailed info → Standard

Height

ZBTB38 · rs9846396

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Height

ST8SIA3 · rs3745060

See detailed info → Standard

Height

PRPF40A · rs4664605

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height (minimum, inv-normal transformed)

MEIS1 · rs12995572

See detailed info → Standard

Height

HHIP-AS1 · rs6845999

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Height (maximum, inv-normal transformed)

near RNU2-36P · rs460177

See detailed info → Standard

Standing height (UKB data field 50)

near MAP2K2 · rs72978905

See detailed info → Standard

Height

CDK6 · rs147826719

See detailed info → Standard

Height (baseline)

PSMA1 · rs34162548

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Showing 20 of 11129 · page 207 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.