Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,083 positions on this site are linked to Height, out of 2,506,337 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 (maximum, inv-normal transformed)

ANKRD9 · rs3742445

See detailed info → Standard

Height

PRDM6 · rs335206

See detailed info → Standard

Height

LINC-PINT · rs12533596

See detailed info → Standard

Height

C17orf82 · rs10853031

See detailed info → Standard

Height (maximum, inv-normal transformed)

VRK2 · rs10171955

See detailed info → Standard

Height

TMEM108 · rs2699869

See detailed info → Standard

Height

near PPIAP24 · rs9555311

See detailed info → Standard

Height

near ITPRID2-DT · rs7592216

See detailed info → Standard

Height

CMIP · rs2966116

See detailed info → Standard

Height

near RNY4P18 · rs1978304

See detailed info → Standard

Height

ZBTB4 · rs3853894

See detailed info → Standard

Height

LALTOP · rs28532847

See detailed info → Standard

Height

near BANF2 · rs6080830

See detailed info → Standard

Height

RHOC · rs2279500

See detailed info → Standard

Height

EBF1 · rs4921518

See detailed info → Standard

Height

NINJ2 · rs9861

See detailed info → Standard

Height

RAB11FIP4 · rs882544

See detailed info → Standard

Height

USP10 · rs7498516

See detailed info → Standard

Height

MEOX2 · rs3801427

See detailed info → Standard

Height

near CASC20 · rs1407039

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Showing 20 of 11083 · page 553 of 555

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.