Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,608 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

NPAS3 · rs1958055

See detailed info → Standard

Height (baseline)

near TPM3P4 · rs17427162

See detailed info → Standard

Height (baseline)

near MIR588 · rs17053981

See detailed info → Standard

Height

ZFHX3 · rs1548373

See detailed info → Standard

Height (baseline)

near FGF18 · rs150329167

See detailed info → Standard

Height

SAMD12-AS1 · rs1493939

See detailed info → Standard

Height

near LINC02866 · rs13275833

See detailed info → Standard

Height (baseline)

near LINC01016 · rs12214568

See detailed info → Standard

Height

FILNC1 · rs12203040

See detailed info → Standard

Height (baseline)

SLC6A4 · rs117390397

See detailed info → Standard

Height (baseline)

near GPR45 · rs11683645

See detailed info → Standard

Height (baseline)

near GUSBP5 · rs116825877

See detailed info → Standard

Height (standard GWA)

LCORL · rs116570344

See detailed info → Standard

Height

near NTRK3-AS1 · rs11631531

See detailed info → Standard

Height (baseline)

POM121L2 · rs116044476

See detailed info → Standard

Height (baseline)

DNM3 · rs115031165

See detailed info → Standard

Height (baseline)

SCP2 · rs11206051

See detailed info → Standard

Height

HELLPAR · rs11111206

See detailed info → Standard

Height

KIF17 · rs10916848

See detailed info → Standard

Height

TRAM2 · rs1056706

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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.