Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,659 positions on this site are linked to Height, out of 2,511,803 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

CCPG1 · rs8027135

See detailed info → Standard

Height

near SLC38A4-AS1 · rs17691793

See detailed info → Standard

Height

POLD3 · rs1655483

See detailed info → Standard

Height

KTN1 · rs12590388

See detailed info → Standard

Height

near FST · rs11954686

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Height

NR3C1 · rs10482682

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Height

TET3 · rs7593050

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Height

PCSK5 · rs10512053

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Height

near RPL31P42 · rs2029247

See detailed info → Standard

Height

near LINC02160 · rs12187304

See detailed info → Standard

Height

near MIR4432HG · rs17329195

See detailed info → Standard

Height (baseline)

STAU1 · rs13039749

See detailed info → Standard

Height

LINC02384 · rs11177270

See detailed info → Standard

Height

PTPRG · rs7625335

See detailed info → Standard

Height

HLX-AS1 · rs3806325

See detailed info → Standard

Height

RPS10-NUDT3 · rs16889678

See detailed info → Standard

Height

near LINC02641 · rs11592827

See detailed info → Standard

Height

CDK14 · rs6465282

See detailed info → Standard

Height

SRBD1 · rs3731946

See detailed info → Standard

Height

near HMGN1P9 · rs3846051

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Showing 20 of 11659 · page 36 of 583

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.