Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,639 positions on this site are linked to Height, out of 2,511,526 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

TLK2 · rs11657101

See detailed info → Standard

Height

GOLGA3 · rs2291256

See detailed info → Standard

Height

PDE3A · rs10841577

See detailed info → Standard

Height

PRRC2A · rs3130623

See detailed info → Standard

Height

LIN28A · rs35015532

See detailed info → Standard

Height

L3MBTL3 · rs6569647

See detailed info → Standard

Height

FNDC3B · rs582780

See detailed info → Standard

Height

near ADAMTS10 · rs4072910

See detailed info → Standard

Height

near ADAMTSL3 · rs2585043

See detailed info → Standard

Height

GNA12 · rs208346

See detailed info → Standard

Height

near RYBP · rs11128264

See detailed info → Standard

Height

IRAIN · rs9672558

See detailed info → Standard

height (mean, inv-normal transformed)

CADPS2 · rs1899690

See detailed info → Standard

height (mean, inv-normal transformed)

FIBIN · rs138273386

See detailed info → Standard

height (mean, inv-normal transformed)

near CASC20 · rs6038570

See detailed info → Standard

Height

SUSD5 · rs6810039

See detailed info → Standard

Height

MGAT3 · rs5757680

See detailed info → Standard

Height

CCDC50 · rs9841435

See detailed info → Standard

Height

MICOS10-NBL1 · rs12408663

See detailed info → Standard

Height

IGF1R · rs2684777

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Showing 20 of 11639 · page 24 of 582

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.