Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,869 positions on this site are linked to Height, out of 113,447 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Height

Standard

Height

MAP3K14 · rs11574836

See detailed info →
Standard

Height (baseline)

CCDC12 · rs114704096

See detailed info →
Standard

Height (baseline)

PCBP1-AS1 · rs113679139

See detailed info →
Standard

Visceral adipose tissue volumes (adjusted for BMI and height)

near HLA-DRB5 · rs113602321

See detailed info →
Standard

Height (baseline)

EVI5 · rs11164771

See detailed info →
Standard

Height (baseline)

ODAD2 · rs11006785

See detailed info →
Standard

Height (baseline)

near KIFBP · rs10998540

See detailed info →
Standard

Height

near LINC02464 · rs10858543

See detailed info →
Standard

Height

SMARCA2 · rs10811579

See detailed info →
Standard

Height

near RNA5SP281 · rs10758127

See detailed info →
Standard

Height

LINC01948 · rs10513081

See detailed info →
Standard

Height

BABAM2 · rs1038694

See detailed info →
Standard

Height

near RN7SL51P · rs10167600

See detailed info →
Standard

Height

LINC01942 · rs10074473

See detailed info →
Standard

Height

FGD4 · rs10047581

See detailed info →
Standard

Height

STX18 · rs10018574

See detailed info →
Standard

Height

near RNU5A-2P · rs10006067

See detailed info →
Standard

Height

LINC02994 · rs9992120

See detailed info →
Standard

Height

near EPHB6 · rs9986701

See detailed info →
Standard

Height

LINC02694 · rs9972581

See detailed info →

Showing 20 of 9869 · page 65 of 494

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.