Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 12, 2026

11,888 positions on this site are linked to Height, out of 2,516,151 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

CCDC9 · rs4804036

See detailed info → Standard

Height

DLEU2 · rs9316484

See detailed info → Standard

Height

NPHP3-ACAD11 · rs7629689

See detailed info → Standard

Height

near FGFR3 · rs1867926

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Height

TTLL5 · rs12147363

See detailed info → Standard

Height

CRADD · rs725574

See detailed info → Standard

Height

DPY19L3 · rs7253808

See detailed info → Standard

Height

near PRKG2 · rs1662840

See detailed info → Standard

Height

TSPAN9 · rs7980313

See detailed info → Standard

Height

COL27A1 · rs4143245

See detailed info → Standard

Height (baseline)

FKBP5 · rs114623987

See detailed info → Standard

Height

ACAN · rs16942318

See detailed info → Standard

Height

near TRIP11 · rs4900092

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Height

CRIM1 · rs17018786

See detailed info → Standard

Height

ZNF536 · rs8101081

See detailed info → Standard

Height

ANKH · rs153920

See detailed info → Standard

Height (baseline)

C2 · rs3020644

See detailed info → Standard

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

near CCN3 · rs76563195

See detailed info → Standard

Height (baseline)

near HMGA2 · rs12810075

See detailed info → Standard

Height

PCOLCE2 · rs2707982

See detailed info →

Showing 20 of 11888 · page 66 of 595

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.