Variants linked to Height

Continuously updated · newest added Oct 23, 2026

9,480 positions on this site are linked to Height, out of 108,914 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

COPB1 · rs79732015

See detailed info →
Standard

Height

ZFAT · rs4909912

See detailed info →
Standard

Height

near Y_RNA · rs16823787

See detailed info →
Standard

Height

near TTC4P1 · rs1540824

See detailed info →
Standard

Height

ESR1 · rs3798758

See detailed info →
Standard

Height

NSF · rs35937770

See detailed info →
Standard

Height

ARID4A · rs10137475

See detailed info →
Standard

Height

near CYP26B1 · rs4852850

See detailed info →
Standard

Height

ZBTB38 · rs9846396

See detailed info →
Standard

Height

ST8SIA3 · rs3745060

See detailed info →
Standard

Height

PRPF40A · rs4664605

See detailed info →
Standard

Height (baseline)

RALY · rs79027916

See detailed info →
Standard

Height

near LINC00691 · rs1112195

See detailed info →
Standard

Height

ABCB1 · rs2032588

See detailed info →
Standard

Height

ZNF799 · rs7246440

See detailed info →
Standard

Height

RNF212 · rs17131824

See detailed info →
Standard

Standing height (UKB data field 50)

near NMBR · rs4128460

See detailed info →
Standard

Height

near RNU6-13P · rs353721

See detailed info →
Standard

Height

ADCY3 · rs2384061

See detailed info →
Standard

Height

KLF2-DT · rs501537

See detailed info →

Showing 20 of 9480 · page 444 of 474

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.