Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,645 positions on this site are linked to Height, out of 2,511,711 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

ZNF423 · rs16947741

See detailed info → Standard

Height

LINC02373 · rs732214

See detailed info → Standard

Height

near SUSD5 · rs4678506

See detailed info → Standard

Height

GLI3 · rs3823734

See detailed info → Standard

Height

near RNU1-96P · rs2643825

See detailed info → Standard

Height

SCFD1 · rs229155

See detailed info → Standard

Height

MIR3681HG · rs11893707

See detailed info → Standard

Height

near DNAJB8-AS1 · rs11718692

See detailed info → Standard

Height

LRBA · rs11933114

See detailed info → Standard

Height (baseline)

MEF2C-AS1 · rs1159666

See detailed info → Standard

Height

TRANK1 · rs9857252

See detailed info → Standard

Height

near RASA2 · rs7611234

See detailed info → Standard

Height

HIVEP1 · rs6916070

See detailed info → Standard

Height

near BMP2 · rs16992673

See detailed info → Standard

Height (baseline)

ZBTB38 · rs73872720

See detailed info → Standard

Height

PDE10A · rs7741165

See detailed info → Standard

Height

FAM83B · rs6911198

See detailed info → Standard

Height

GFPT2 · rs6869637

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Height

near LINC02871 · rs6040264

See detailed info → Standard

Height

near PITX1 · rs31210

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Showing 20 of 11645 · page 29 of 583

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.