Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,083 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

Height

RAX · rs2271733

See detailed info → Standard

Height

near CNTF · rs61889537

See detailed info → Standard

Height

MIR17HG · rs9523313

See detailed info → Standard

Height (baseline)

KIF9 · rs56273245

See detailed info → Standard

Height

SUCLA2P3 · rs17801121

See detailed info → Standard

Height (baseline)

near KRT17P3 · rs149237084

See detailed info → Standard

Height

CAHM · rs4709714

See detailed info → Standard

Height

near RPL22P19 · rs7971677

See detailed info → Standard

Height

ACO2 · rs738140

See detailed info → Standard

Height (baseline)

near VPS51P17 · rs308350

See detailed info → Standard

Height

BMP6 · rs9392918

See detailed info → Standard

Height (baseline)

TSC2 · rs13334473

See detailed info → Standard

Height (baseline)

near TBX4 · rs71373880

See detailed info → Standard

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

CDCA2 · rs73220082

See detailed info → Standard

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

MPHOSPH6 · rs6420434

See detailed info → Standard

Height

HMGA2 · rs17179670

See detailed info → Standard

Height

near CYP1A1 · rs12441817

See detailed info → Standard

Height (baseline)

PIGC · rs111949353

See detailed info → Standard

Height

CCDC12 · rs61509315

See detailed info → Standard

height (minimum, inv-normal transformed)

BCKDHB · rs4446525

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Showing 20 of 11083 · page 190 of 555

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.