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 8, 2026

10,926 positions on this site are linked to Height, out of 2,505,576 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

SOCS2-AS1 · rs10777527

See detailed info → Standard

Height

PRMT1 · rs10415880

See detailed info → Standard

Height (baseline)

ADAMTS17 · rs4627319

See detailed info → Standard

Height

GMDS · rs10484693

See detailed info → Standard

Height

C1QTNF7-AS1 · rs9991734

See detailed info → Standard

Height

SNX10 · rs7782538

See detailed info → Standard

Height

near LINC02113 · rs7708256

See detailed info → Standard

Height

near SSRP1 · rs7110052

See detailed info → Standard

Height

HAO1 · rs941425

See detailed info → Standard

Height

TUBA4A · rs6707873

See detailed info → Standard

Height

CMIP · rs3935338

See detailed info → Standard

Height

CREBRF · rs251248

See detailed info → Standard

Height

KCNE2 · rs12626741

See detailed info → Standard

Height

ANKLE1 · rs891018

See detailed info → Standard

Standing height (UKB data field 50)

near CRADD · rs7961023

See detailed info → Standard

Height

RORA · rs7168905

See detailed info → Standard

Height

LINC01755 · rs709397

See detailed info → Standard

Height

MOCS1 · rs2273853

See detailed info → Standard

Height

SMG9 · rs2074634

See detailed info → Standard

Height

near PLCL1 · rs1996464

See detailed info →

Showing 20 of 10926 · page 138 of 547

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.