Gene Knowledge Graph

UTC

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 8, 2026

11,227 positions on this site are linked to Height, out of 2,507,279 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

MIRLET7BHG · rs3744749

See detailed info → Standard

Height

near ANKS3 · rs841217

See detailed info → Standard

Height

near RN7SL7P · rs2188177

See detailed info → Standard

Height (baseline)

CCDC91 · rs11049376

See detailed info → Standard

height (mean, inv-normal transformed)

ADAMTSL3 · rs11855967

See detailed info → Standard

Height

RMND1 · rs7771156

See detailed info → Standard

Height

PLPPR1 · rs4998243

See detailed info → Standard

Height

near TRMT44 · rs1949733

See detailed info → Standard

height (minimum, inv-normal transformed)

near PRKG2 · rs3098970

See detailed info → Standard

Height

CMIP · rs2966116

See detailed info → Standard

Height

near RNY4P18 · rs1978304

See detailed info → Standard

Height

ZBTB4 · rs3853894

See detailed info → Standard

Height

LALTOP · rs28532847

See detailed info → Standard

Height

near BANF2 · rs6080830

See detailed info → Standard

Height

RHOC · rs2279500

See detailed info → Standard

Height

EBF1 · rs4921518

See detailed info → Standard

Height

NINJ2 · rs9861

See detailed info → Standard

Height

RAB11FIP4 · rs882544

See detailed info → Standard

Height

USP10 · rs7498516

See detailed info → Standard

Height

MEOX2 · rs3801427

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.