Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,468 positions on this site are linked to Height, out of 2,509,439 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

PROM1 · rs4698432

See detailed info → Standard

Height (baseline)

FANCC · rs4647394

See detailed info → Standard

Height (baseline)

URAHP · rs4628973

See detailed info → Standard

Height

KCNQ5 · rs4582343

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Height

near LSM3 · rs4575884

See detailed info → Standard

Height (baseline)

ZSWIM5 · rs4484960

See detailed info → Standard

Height

VCL · rs4414157

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Height

near BPGM · rs4269477

See detailed info → Standard

Height

MIR4280HG · rs40466

See detailed info → Standard

Height

near KPNA3 · rs3903768

See detailed info → Standard

Height

PCOLCE2 · rs3816690

See detailed info → Standard

Height

TTC23 · rs3743241

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Height

POLR2B · rs3733309

See detailed info → Standard

Height (baseline)

near CFL1 · rs369581563

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Height (baseline)

ICAM5 · rs36045754

See detailed info → Standard

Height (baseline)

MECOM · rs35296325

See detailed info → Standard

Height (baseline)

LINC02829 · rs35174396

See detailed info → Standard

Height (baseline)

near ATP5MGP4 · rs35024157

See detailed info → Standard

Height (baseline)

NEO1 · rs34386426

See detailed info → Standard

Height (standard GWA)

SLC22A20P · rs34267485

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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.