Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 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

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

See detailed info → Standard

Height

ITIH3 · rs2710329

See detailed info → Standard

Height

TTC13 · rs16853414

See detailed info → Standard

Height

HIVEP2 · rs12212322

See detailed info → Standard

Height (baseline)

ZKSCAN3 · rs72854536

See detailed info → Standard

Height

WNT3 · rs3916033

See detailed info → Standard

Height

near PNCRNA-D · rs3212861

See detailed info → Standard

Height (baseline)

TRPC4AP · rs79965102

See detailed info → Standard

Height

EBF3 · rs10829665

See detailed info → Standard

Height (baseline)

SLC26A8 · rs540188223

See detailed info → Standard

Height (baseline)

FAF1-AS1 · rs1278523

See detailed info → Standard

height (minimum, inv-normal transformed)

P4HA2 · rs11955347

See detailed info → Standard

Height

near LINC00924 · rs16973982

See detailed info → Standard

Height

RUNX2 · rs1200426

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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.