Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,319 positions on this site are linked to Height, out of 107,306 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

C3orf49 · rs2130990

See detailed info →
Standard

Height

ZNF638 · rs2287326

See detailed info →
Standard

Height

MATN2 · rs2290472

See detailed info →
Standard

Height

SMCHD1 · rs2347808

See detailed info →
Standard

Height

near STXBP4 · rs2529518

See detailed info →
Standard

Height

RFT1 · rs2564924

See detailed info →
Standard

Height

NRXN3 · rs2574750

See detailed info →
Standard

Height

PCGF5 · rs2631676

See detailed info →
Standard

Height

near TET2 · rs2647251

See detailed info →
Standard

Height

GFRA1 · rs2694765

See detailed info →
Standard

Height

near HDAC11 · rs2731341

See detailed info →
Standard

Height

near SMOC2 · rs2763263

See detailed info →
Standard

Height

SLC2A13 · rs28370628

See detailed info →
Standard

Height

RILPL2 · rs28410896

See detailed info →
Standard

Height

B3GNT8 · rs284661

See detailed info →
Standard

Height

near IMPA2 · rs2849412

See detailed info →
Standard

Height

GHRHR · rs28710006

See detailed info →
Standard

Height

near ZNF648 · rs3856113

See detailed info →
Standard

Height

TTC23L · rs3857367

See detailed info →
Standard

Height

near BMP2 · rs4142037

See detailed info →

Showing 20 of 9319 · page 454 of 466

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.