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 11, 2026

11,679 positions on this site are linked to Height, out of 2,512,094 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

Standard

Height

near ACE3P · rs8075924

See detailed info →
Standard

Height

CYP19A1 · rs10519301

See detailed info →
Standard

Height

near ROR2 · rs16907585

See detailed info →
Standard

Height

YRDC · rs3795494

See detailed info →
Standard

Height

GMDS · rs7751738

See detailed info →
Standard

Height

AGXT · rs12695032

See detailed info →
Standard

Height

MRPL42 · rs9943803

See detailed info →
Standard

Height

near MIR30B · rs7827871

See detailed info →
Standard

Height

near RPS4XP9 · rs9385404

See detailed info →
Standard

Height

near RN7SKP93 · rs6716309

See detailed info →
Standard

Height

near MIR17HG · rs9589196

See detailed info →
Standard

Height

MAP4 · rs2230169

See detailed info →
Standard

Height

BABAM2 · rs7558946

See detailed info →
Standard

Height

CLASP2 · rs6796857

See detailed info →
Standard

Height

STAG1-DT · rs1533445

See detailed info →
Standard

Height

H2BC6 · rs17533076

See detailed info →
Standard

Height

COLGALT2 · rs9970117

See detailed info →
Standard

Height

near MC3R · rs6064361

See detailed info →
Standard

Height

CHD1L · rs9661159

See detailed info →
Standard

Height

MED13L · rs7969182

See detailed info →

Showing 20 of 11679 · page 56 of 584

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.