Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

4,645 positions on this site are linked to Height, out of 2,509,834 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 (minimum, inv-normal transformed)

FLI1 · rs612282

See detailed info → Standard

Height (baseline)

CASC20 · rs6117293

See detailed info → Standard

Height

near MIR548A1HG · rs17629312

See detailed info → Standard

Height

HHIP · rs1355601

See detailed info → Standard

Height

LHPP · rs10794146

See detailed info → Standard

Height

LY75 · rs2042772

See detailed info → Standard

Height

SMG6 · rs1885987

See detailed info → Standard

Height

USP34 · rs778160

See detailed info → Standard

Height

DLEU1 · rs9535499

See detailed info → Standard

Height

PRR16 · rs1404300

See detailed info → Standard

Height

MKLN1 · rs10954312

See detailed info → Standard

Height

PDE10A · rs221730

See detailed info → Standard

Height

FNDC3B · rs1039027

See detailed info → Standard

Height

CDKN2B-AS1 · rs944802

See detailed info → Standard

Height

near U3 · rs916893

See detailed info → Standard

Height

CYP19A1 · rs2445761

See detailed info → Standard

Height

CDC42EP3-AS1 · rs17021261

See detailed info → Standard

Height

HIPK2 · rs11770283

See detailed info → Standard

Height

near RPL37P6 · rs11990963

See detailed info → Standard

Height

near NUP37 · rs11111147

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Showing 20 of 4645 · page 2 of 233

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.