Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,771 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 CCDC12 · rs114404763

See detailed info → Standard

Height

GPR135 · rs113239787

See detailed info → Standard

Height

CS · rs11171792

See detailed info → Standard

Height

CCBE1 · rs11152156

See detailed info → Standard

Height

ABI1 · rs10829061

See detailed info → Standard

Height (standard GWA)

near ALDH7A1P4 · rs10822054

See detailed info → Standard

Height (standard GWA)

near MRPL42 · rs10777513

See detailed info → Standard

Height

FKBP9 · rs10266139

See detailed info → Standard

Height (baseline)

near RN7SKP277 · rs10240344

See detailed info → Standard

Height (standard GWA)

AMZ2 · rs9944517

See detailed info → Standard

Height

LINC00870 · rs9917816

See detailed info → Standard

Height (baseline)

NFIC · rs9748965

See detailed info → Standard

Height

TRAM2 · rs941969

See detailed info → Standard

Height (baseline)

SYNE1 · rs9397486

See detailed info → Standard

Height (baseline)

near CYB5B · rs8054363

See detailed info → Standard

Height (baseline)

TRMT1L · rs79919395

See detailed info → Standard

Height (baseline)

DUSP16 · rs79687643

See detailed info → Standard

Height (baseline)

FNIP1 · rs79577858

See detailed info → Standard

Height (baseline)

MRPL23 · rs7945810

See detailed info → Standard

Height

UBASH3B · rs7940959

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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.