Gene Knowledge Graph

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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,432 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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

← Back to Height

Height (baseline)

HLA-DQA1 · rs150752156

See detailed info → Standard

Height (baseline)

NBEAL2 · rs73075647

See detailed info → Standard

Height

near PIK3R1 · rs11750646

See detailed info → Standard

Height

near MIR422A · rs11631933

See detailed info → Standard

Height

ZNF76 · rs6919534

See detailed info → Standard

Height (baseline)

DNAJC27 · rs62140616

See detailed info → Standard

Height (baseline)

SH2D5 · rs113664832

See detailed info → Standard

Height (baseline)

CCDC91 · rs3963302

See detailed info → Standard

Height

ANAPC10 · rs17725458

See detailed info → Standard

Height

near SPSB1 · rs658997

See detailed info → Standard

Height

DYM · rs16950303

See detailed info → Standard

Height

ADAMTS6 · rs16893717

See detailed info → Standard

Height

SLC24A3 · rs3827975

See detailed info → Standard

Height

LILRB5 · rs2361797

See detailed info → Standard

Height

SOX2-OT · rs35788479

See detailed info → Standard

Height

near ANAPC16 · rs12266147

See detailed info → Standard

Height (baseline)

AAR2 · rs2425193

See detailed info → Standard

Standing height (UKB data field 50)

near LINC01488 · rs872440

See detailed info → Standard

Height

near PTCH1 · rs28393820

See detailed info → Standard

Height (baseline)

near LINC02947 · rs13263338

See detailed info →

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.