Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,344 positions on this site are linked to Height, out of 2,508,253 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)

near ARFGEF2 · rs3092395

See detailed info → Standard

Standing height (UKB data field 50)

MIR3183 · rs2663345

See detailed info → Standard

height (minimum, inv-normal transformed)

NGF-AS1 · rs2747063

See detailed info → Standard

Height (baseline)

near PNMA8A · rs10403206

See detailed info → Standard

Height

near RN7SKP93 · rs7574116

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height (mean, inv-normal transformed)

ZBTB20 · rs116680082

See detailed info → Standard

Height

BBS9 · rs1451018

See detailed info → Standard

Height

LINC01934 · rs6750529

See detailed info → Standard

Height

near NPY1R · rs4146926

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Height

PLEKHM3 · rs10497888

See detailed info → Standard

Height

MECOM · rs1997280

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Standing height (UKB data field 50)

LINC03007 · rs79197311

See detailed info → Standard

Height (baseline)

CTNNB1 · rs1722845

See detailed info → Standard

Pericardial adipose tissue adjusted for height and weight

TRIB2 · rs10198628

See detailed info → Standard

Height

near RNU4-76P · rs58972372

See detailed info → Standard

Height

FILIP1 · rs12212816

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Height (baseline)

FNDC3B · rs9812159

See detailed info → Standard

height (minimum, inv-normal transformed)

LUZP1 · rs2806558

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height (mean, inv-normal transformed)

near LATS2 · rs7326823

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Height

RXRG · rs466639

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Showing 20 of 11344 · page 228 of 568

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.