Gene Knowledge Graph

UTC

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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,344 positions on this site are linked to Height, out of 2,508,301 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Height

CLEC4M · rs874492

See detailed info → Standard

Height

DLX6-AS1 · rs56363908

See detailed info → Standard

Height

GPC5 · rs7319045

See detailed info → Standard

Height

near DCUN1D4 · rs2102278

See detailed info → Standard

Height

MORC3 · rs113382956

See detailed info → Standard

height (mean, inv-normal transformed)

BRD3 · rs2520099

See detailed info → Standard

Height

REEP5 · rs153560

See detailed info → Standard

Height

DCST1 · rs74520550

See detailed info → Standard

Height

LTBP1 · rs6714546

See detailed info → Standard

Height

CYP19A1 · rs28566535

See detailed info → Standard

Height

MEF2C · rs10037512

See detailed info → Standard

Height

ADAMTSL3 · rs8024628

See detailed info → Standard

Height

near CTDSP2 · rs10747787

See detailed info → Standard

Height

near FGFR1 · rs881301

See detailed info → Standard

height (mean, inv-normal transformed)

CHD4 · rs7310535

See detailed info → Standard

Height

FGFR4 · rs422421

See detailed info → Standard

Height

AMZ1 · rs798491

See detailed info → Standard

Height

ANKS1A · rs13210323

See detailed info → Standard

Height

HOXD3 · rs4972504

See detailed info → Standard

Height

near ADAMTS3 · rs4694504

See detailed info →

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.