Gene Knowledge Graph

UTC

Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,487 positions on this site are linked to Height, out of 2,509,560 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 (baseline)

near CPLX2 · rs4867813

See detailed info → Standard

Height (baseline)

AAK1 · rs4852898

See detailed info → Standard

Height

FHOD3 · rs4349223

See detailed info → Standard

Height (baseline)

PDXDC2P-NPIPB14P · rs377753719

See detailed info → Standard

Height (baseline)

near LYNX1-SLURP2 · rs373472791

See detailed info → Standard

Height

RUSC1 · rs35117735

See detailed info → Standard

Height (baseline)

TMEM50A · rs3093599

See detailed info → Standard

Height (standard GWA)

near CDK5RAP1 · rs291668

See detailed info → Standard

Height (baseline)

near LINC02872 · rs28579234

See detailed info → Standard

Height

MATN2 · rs28524918

See detailed info → Standard

Height

PKD1L1 · rs2686821

See detailed info → Standard

Height (baseline)

MYPN · rs2673801

See detailed info → Standard

Height

H2BK1 · rs2608291

See detailed info → Standard

Height

near LINP1 · rs2486866

See detailed info → Standard

Height (baseline)

near DYSF · rs1961080

See detailed info → Standard

Height (baseline)

near MIR548A1HG · rs186456569

See detailed info → Standard

Height (baseline)

LTBP1 · rs183831977

See detailed info → Standard

Height

near LINC02100 · rs183093602

See detailed info → Standard

Height

near HTR1A · rs17181344

See detailed info → Standard

Height

NXNL2 · rs17054242

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.