Gene Knowledge Graph
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Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,486 positions on this site are linked to Height, out of 2,509,486 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 (standard GWA)

near SUPT3H · rs546936

See detailed info → Standard

Height (baseline)

POU2F3 · rs533042277

See detailed info → Standard

Height

near NPPC · rs5262

See detailed info → Standard

Height

RAI1 · rs4925112

See detailed info → Standard

Height

near LGI1 · rs4919543

See detailed info → Standard

Height

LINC01524 · rs4811379

See detailed info → Standard

Height

SULF2 · rs4809646

See detailed info → Standard

Height

near CELF2-DT · rs4747860

See detailed info → Standard

Height

near LINC01331 · rs4703635

See detailed info → Standard

Height

near LINC00607 · rs4672773

See detailed info → Standard

Height (baseline)

WARS2-AS1 · rs4659152

See detailed info → Standard

Height

near VANGL2 · rs4656258

See detailed info → Standard

Height

ANKRD44 · rs4435471

See detailed info → Standard

Height

near FIGN · rs4145983

See detailed info → Standard

Height

PIK3C2A · rs3950680

See detailed info → Standard

Height

near RNU7-93P · rs3909618

See detailed info → Standard

Height (baseline)

CRADD · rs381492

See detailed info → Standard

Height

TACR1 · rs3771863

See detailed info → Standard

Height (baseline)

PTGFR · rs3766333

See detailed info → Standard

Height (baseline)

CDK6 · rs3731360

See detailed info →

Showing 20 of 11486 · page 271 of 575

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.