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 2,509,343 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 (baseline)

near SLC9A1 · rs72651596

See detailed info → Standard

Height

near BANF2 · rs7261451

See detailed info → Standard

Height

CHFR · rs725067

See detailed info → Standard

Height (baseline)

LINC03111 · rs7238234

See detailed info → Standard

Height

ZNF521 · rs7234082

See detailed info → Standard

Height (baseline)

near LINC01497 · rs7224968

See detailed info → Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

RELA-DT · rs71455776

See detailed info → Standard

Height

near CDK1 · rs7093851

See detailed info → Standard

Height (baseline)

near MIR4682 · rs7090910

See detailed info → Standard

Height

LINC01592 · rs683567

See detailed info → Standard

Height (baseline)

GPR78 · rs6817637

See detailed info → Standard

Height (baseline)

ARHGAP31 · rs6796981

See detailed info → Standard

Height

CMSS1 · rs6792339

See detailed info → Standard

Height (baseline)

RYK · rs66562242

See detailed info → Standard

Height

DNMBP · rs6584331

See detailed info → Standard

Height

near ZNF827 · rs6537382

See detailed info → Standard

Height (standard GWA)

near MIR8070 · rs6485214

See detailed info → Standard

Height (baseline)

PCAT1 · rs6470486

See detailed info → Standard

Height

COL24A1 · rs641712

See detailed info → Standard

Height (baseline)

near LINC03005 · rs62389289

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Showing 20 of 11468 · page 257 of 574

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.