Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,464 positions on this site are linked to Height, out of 2,509,249 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 TBX2-AS1 · rs9913946

See detailed info → Standard

Height

CASC20 · rs6117342

See detailed info → Standard

Height (baseline)

E2F7 · rs2369463

See detailed info → Standard

Height (baseline)

ESR1 · rs2175898

See detailed info → Standard

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

EIF2AK3 · rs13001657

See detailed info → Standard

Height

ANGPT1 · rs1283688

See detailed info → Standard

Height (baseline)

STAB1 · rs1010552

See detailed info → Standard

Height (baseline)

near DNM1P51 · rs3803392

See detailed info → Standard

Height (baseline)

near RPL21P71 · rs1814982

See detailed info → Standard

Height

near AMD1 · rs1704721

See detailed info → Standard

Height

CDK6 · rs10488521

See detailed info → Standard

Height

TNS1 · rs2552527

See detailed info → Standard

Height

WWOX · rs8052110

See detailed info → Standard

Height (baseline)

FBXW8 · rs4238050

See detailed info → Standard

Height

TENM3 · rs17309350

See detailed info → Standard

Height

near RPSAP72 · rs1902070

See detailed info → Standard

Height (baseline)

LYN · rs7002888

See detailed info → Standard

Height

PLCB1 · rs12625192

See detailed info → Standard

Height

CBLB · rs12486371

See detailed info → Standard

Height (maximum, inv-normal transformed)

ATP6V0A1 · rs8069972

See detailed info →

Showing 20 of 11464 · page 570 of 574

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.