Variants linked to Height

Continuously updated · newest added Oct 25, 2026

10,116 positions on this site are linked to Height, out of 116,514 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

PLA2G6 · rs4820315

See detailed info →
Standard

Height

near LRRC30 · rs4355009

See detailed info →
Standard

Height (baseline)

SLC7A1 · rs3783260

See detailed info →
Standard

Height

near KIAA0040 · rs3753555

See detailed info →
Standard

Height (baseline)

SAMD3 · rs34209761

See detailed info →
Standard

Height

ZC3H11A · rs34027291

See detailed info →
Standard

Height (baseline)

near LINC02784 · rs299856

See detailed info →
Standard

Height

LINC02694 · rs2929681

See detailed info →
Standard

Height

KIAA2013 · rs2639453

See detailed info →
Standard

Height (baseline)

DAAM2 · rs2504797

See detailed info →
Standard

Height (baseline)

near RNPC3-DT · rs2376357

See detailed info →
Standard

Height (baseline)

DNAH10 · rs202015039

See detailed info →
Standard

Height (baseline)

near SLC28A1 · rs201090642

See detailed info →
Standard

Height (baseline)

ANKS1A · rs186447074

See detailed info →
Standard

Height

near RMST · rs17387773

See detailed info →
Standard

Height

FOXP1 · rs17008175

See detailed info →
Standard

Height (baseline)

near RN7SKP46 · rs16828455

See detailed info →
Standard

Height (baseline)

CDC25C · rs150985593

See detailed info →
Standard

Height

near ZNF619P1 · rs1486146

See detailed info →
Standard

Height (baseline)

HLA-DRB6 · rs145740519

See detailed info →

Showing 20 of 10116 · page 98 of 506

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.