Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,668 positions on this site are linked to Height, out of 2,512,094 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

DOT1L · rs7256735

See detailed info → Standard

Height

FOSL1 · rs10791830

See detailed info → Standard

Height

near DCDC1 · rs10767874

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Height

MIR4713HG · rs10519302

See detailed info → Standard

Height

TET2 · rs6533181

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Height

COL24A1 · rs17400787

See detailed info → Standard

Height

ZNF143 · rs11042366

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Height

PCSK6 · rs765825

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Height

near PRRX1 · rs501680

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height (mean, inv-normal transformed)

near GH2 · rs2727317

See detailed info → Standard

Height

LOXL2 · rs4872112

See detailed info → Standard

Height

PSMD5 · rs12343516

See detailed info → Standard

Height

CRK-AS1 · rs6502670

See detailed info → Standard

Height

near NR5A2 · rs2246072

See detailed info → Standard

Height

GNAS · rs6026576

See detailed info → Standard

Height

near LINC00536 · rs4876357

See detailed info → Standard

Height

ADAMTS17 · rs1351438

See detailed info → Standard

Height

ARSJ · rs13110620

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Height

near TSPAN3 · rs11856538

See detailed info → Standard

Height

LINC01102 · rs11123995

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Showing 20 of 11668 · page 15 of 584

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.