Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,083 positions on this site are linked to Height, out of 2,506,243 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height (baseline)

near HLA-DQB1 · rs28483633

See detailed info → Standard

Height

ZZEF1 · rs17175885

See detailed info → Standard

Height

GIGYF1 · rs221795

See detailed info → Standard

Height

near RAMP3 · rs1294847

See detailed info → Standard

Height

MXD1 · rs4853173

See detailed info → Standard

height (mean, inv-normal transformed)

JHY · rs4293127

See detailed info → Standard

Standing height (UKB data field 50)

VPS13C · rs12594946

See detailed info → Standard

Height (baseline)

CDK6-AS1 · rs77489095

See detailed info → Standard

Height (baseline)

TENT5A · rs75451347

See detailed info → Standard

Height (baseline)

near NMB · rs531061098

See detailed info → Standard

Height (baseline)

WNT5A · rs815540

See detailed info → Standard

Height (baseline)

RALY · rs75912699

See detailed info → Standard

Height (baseline)

CHRNB1 · rs530436279

See detailed info → Standard

Height (baseline)

ZSCAN2-AS1 · rs3762168

See detailed info → Standard

Height

PRRX1 · rs2213751

See detailed info → Standard

Height (baseline)

near U6 · rs140282896

See detailed info → Standard

Height (standard GWA)

ZNF628 · rs73057171

See detailed info → Standard

Height

CMIP · rs6564905

See detailed info → Standard

Height

near MRPS11P1 · rs4814999

See detailed info → Standard

Standing height (UKB data field 50)

near LINC02571 · rs113300871

See detailed info →

Showing 20 of 11083 · page 183 of 555

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.