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

PLEKHM3 · rs10497888

See detailed info → Standard

Height

MECOM · rs1997280

See detailed info → Standard

Standing height (UKB data field 50)

LINC03007 · rs79197311

See detailed info → Standard

Height (baseline)

CTNNB1 · rs1722845

See detailed info → Standard

Pericardial adipose tissue adjusted for height and weight

TRIB2 · rs10198628

See detailed info → Standard

Height

near RNU4-76P · rs58972372

See detailed info → Standard

Height

FILIP1 · rs12212816

See detailed info → Standard

Height (baseline)

FNDC3B · rs9812159

See detailed info → Standard

height (minimum, inv-normal transformed)

LUZP1 · rs2806558

See detailed info → Standard

height (mean, inv-normal transformed)

near LATS2 · rs7326823

See detailed info → Standard

Height

RXRG · rs466639

See detailed info → Standard

Height (baseline)

ANAPC10 · rs559931366

See detailed info → Standard

Height

near NUCKS1 · rs55735020

See detailed info → Standard

height (mean, inv-normal transformed)

PVT1 · rs10808567

See detailed info → Standard

Height (maximum, inv-normal transformed)

ZNF483 · rs10217747

See detailed info → Standard

Height (baseline)

near FGFR2 · rs7902581

See detailed info → Standard

Height

ZNF518A · rs61856978

See detailed info → Standard

Height

near MKRN3 · rs117686021

See detailed info → Standard

height (mean, inv-normal transformed)

near RNU2-14P · rs34184001

See detailed info → Standard

Height (baseline)

SMARCD2 · rs547608433

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.