Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,207 positions on this site are linked to Height, out of 106,340 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

IPPK · rs9969804

See detailed info →
Standard

Height

KCNJ12 · rs4640244

See detailed info →
Standard

Height

NUCB2 · rs1330

See detailed info →
Standard

Height

DNAJC27 · rs4665736

See detailed info →
Standard

Height

SOCS5 · rs12474201

See detailed info →
Standard

Height

IGF2BP2 · rs720390

See detailed info →
Standard

Height

SLBP/FGFR3 · rs2247341

See detailed info →
Standard

Height

LIN28 · rs7532866

See detailed info →
Standard

Height

NME2 · rs4605213

See detailed info →
Standard

Height

C2CD4A · rs7178424

See detailed info →
Standard

Height

TREH · rs494459

See detailed info →
Standard

Height

DTL · rs10863936

See detailed info →
Standard

Height

PAPPA2 · rs1325598

See detailed info →
Standard

Height

PIP4K2B · rs1043515

See detailed info →
Standard

Height

PDS5B/BRCA2 · rs7332115

See detailed info →
Standard

Height

TEAD1 · rs7926971

See detailed info →
Standard

Height

RHOD · rs7112925

See detailed info →
Standard

Height

CS · rs3816804

See detailed info →
Standard

Height

QSOX2 · rs7849585

See detailed info →
Standard

Height

MYO9B · rs2279008

See detailed info →

Showing 20 of 9207 · page 459 of 461

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.