Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,181 positions on this site are linked to Height, out of 2,507,049 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 SYNGR2 · rs9900387

See detailed info → Standard

Height

near LINC02995 · rs2112676

See detailed info → Standard

height (mean, inv-normal transformed)

near TLX2 · rs1859734

See detailed info → Standard

Standing height (UKB data field 50)

near SNORD28B · rs7758644

See detailed info → Standard

Height (baseline)

near HLA-DRB9 · rs192091605

See detailed info → Standard

Height

DLG5 · rs149380977

See detailed info → Standard

height (mean, inv-normal transformed)

ERC1 · rs11061744

See detailed info → Standard

Standing height (UKB data field 50)

PAPPA · rs55760822

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Height

near KLF15 · rs9862203

See detailed info → Standard

Height

near USP21P1 · rs978887

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height (mean, inv-normal transformed)

LINC02089 · rs1355680

See detailed info → Standard

Height (baseline)

near ARFGEF2 · rs3092395

See detailed info → Standard

Standing height (UKB data field 50)

MIR3183 · rs2663345

See detailed info → Standard

height (minimum, inv-normal transformed)

NGF-AS1 · rs2747063

See detailed info → Standard

Height (baseline)

near PNMA8A · rs10403206

See detailed info → Standard

Height

near RN7SKP93 · rs7574116

See detailed info → Standard

height (mean, inv-normal transformed)

ZBTB20 · rs116680082

See detailed info → Standard

Height

BBS9 · rs1451018

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Height

LINC01934 · rs6750529

See detailed info → Standard

Height

near NPY1R · rs4146926

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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.