Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,335 positions on this site are linked to Height, out of 2,508,158 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 (baseline)

FIG4 · rs11153213

See detailed info → Standard

Height

MRPS22 · rs16848785

See detailed info → Standard

Height

near LINC01625 · rs17513809

See detailed info → Standard

Height

near USP7 · rs964006

See detailed info → Standard

height (mean, inv-normal transformed)

CCDC91 · rs11049415

See detailed info → Standard

Height

CCND2 · rs3217795

See detailed info → Standard

Height (baseline)

near NPR3 · rs62368123

See detailed info → Standard

Height (baseline)

LINC03135 · rs6931945

See detailed info → Standard

Height

KBTBD2 · rs117701289

See detailed info → 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

See detailed info → Standard

Height

near Y_RNA · rs16823787

See detailed info → Standard

Height

near TTC4P1 · rs1540824

See detailed info → Standard

Height

ESR1 · rs3798758

See detailed info → Standard

Height

NSF · rs35937770

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Height

ARID4A · rs10137475

See detailed info → Standard

Height

near CYP26B1 · rs4852850

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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.