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.

Clear
Recommended (connected, strongest) Strongest evidence Newest Oldest

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)

LBH · rs72787764

See detailed info → Standard

Height

CDC42SE1 · rs6694357

See detailed info → Standard

Height

near LINC01956 · rs651477

See detailed info → Standard

Height

near ZNF563 · rs6511787

See detailed info → Standard

Height (baseline)

AOPEP · rs634851

See detailed info → Standard

Height (baseline)

HSDL2-AS1 · rs62567816

See detailed info → Standard

Height (baseline)

near DYNC1I2 · rs62181736

See detailed info → Standard

Height

near LINC01752 · rs6077955

See detailed info → Standard

Height

CECR3 · rs5994231

See detailed info → Standard

Height (baseline)

DNMT3A · rs560700489

See detailed info → Standard

Height (standard GWA)

AKAP9 · rs4729017

See detailed info → Standard

Height

near NME6 · rs4336143

See detailed info → Standard

Height

near LINC00323 · rs4297971

See detailed info → Standard

Height

near PHB2P1 · rs4083576

See detailed info → Standard

Height

CMTM4 · rs355971

See detailed info → Standard

Height (baseline)

ARSB · rs35516119

See detailed info → Standard

Height

ANKS6 · rs337580

See detailed info → Standard

Height

near ZNF766 · rs2657930

See detailed info → Standard

Height (baseline)

CLNK · rs2531182

See detailed info → Standard

Height (baseline)

near LINC01968 · rs2410887

See detailed info →

Showing 20 of 11487 · page 281 of 575

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.