Gene Knowledge Graph

UTC

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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Height

PTPN14 · rs4472734

See detailed info → Standard

Height

near TRIP11 · rs10129429

See detailed info → Standard

Standing height (UKB data field 50)

ARID5B · rs4245596

See detailed info → Standard

Height

near MAP2K2 · rs350818

See detailed info → Standard

Height

SLC7A1 · rs61947180

See detailed info → Standard

height (mean, inv-normal transformed)

GLCCI1 · rs37983

See detailed info → Standard

Height

SMIM29-AS1 · rs9469762

See detailed info → Standard

Height

FOXN2 · rs76154567

See detailed info → Standard

Height

near UNCX · rs58063923

See detailed info → Standard

Height

SMURF1 · rs12531875

See detailed info → Standard

Height

near TACC3 · rs28528964

See detailed info → Standard

Height

PTPRJ/SLC39A13 · rs10838801

See detailed info → Standard

Height

SCMH1 · rs2154319

See detailed info → Standard

Height

BNC2 · rs1319424

See detailed info → Standard

Height

ZMIZ1 · rs1815314

See detailed info → Standard

Height (maximum, inv-normal transformed)

SRBD1 · rs17033679

See detailed info → Standard

Height

near TRPM8 · rs4663983

See detailed info → Standard

Height

POGK · rs2272792

See detailed info → Standard

height (minimum, inv-normal transformed)

LINC00881 · rs12495519

See detailed info → Standard

Height

C3orf49 · rs832187

See detailed info →

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.