Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,048 positions on this site are linked to Height, out of 2,506,152 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

Standing height (UKB data field 50)

near TMEM244 · rs17755849

See detailed info → Standard

Height (baseline)

near NCL · rs12992177

See detailed info → Standard

Height

RARB · rs1286657

See detailed info → Standard

Height (baseline)

CRADD · rs11107205

See detailed info → Standard

Height

CNN2 · rs10419072

See detailed info → Standard

Height (baseline)

MYH6 · rs10135780

See detailed info → Standard

Height

near HABP4 · rs7870106

See detailed info → Standard

Height (standard GWA)

TMBIM7P · rs75358242

See detailed info → Standard

Height

near SEC16B · rs6670873

See detailed info → Standard

Height (baseline)

near SPATA31C2 · rs56204245

See detailed info → Standard

Height (baseline)

PHF20 · rs539279872

See detailed info → Standard

Standing height (UKB data field 50)

near MIR3622B · rs2439497

See detailed info → Standard

Height

INPP5B · rs2170169

See detailed info → Standard

Height (baseline)

LINC01118 · rs1902320

See detailed info → Standard

Height

HMGA1 · rs138997002

See detailed info → Standard

Height

BBS7 · rs13152701

See detailed info → Standard

Height

MBNL1 · rs13082076

See detailed info → Standard

Height (baseline)

near IGF2BP1 · rs111814912

See detailed info → Standard

Height

PAPPA2 · rs10753130

See detailed info → Standard

Height

LINC02934 · rs7583237

See detailed info →

Showing 20 of 11048 · page 178 of 553

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.