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

11,491 positions on this site are linked to Height, out of 2,509,608 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

RASGEF1B · rs10024084

See detailed info → Standard

Height

LINC01182 · rs10007245

See detailed info → Standard

Height

LINC02469 · rs10002178

See detailed info → Standard

Height

LINC01639 · rs9608024

See detailed info → Standard

Height

near SMLR1 · rs9321251

See detailed info → Standard

Height (baseline)

DOCK3 · rs9311464

See detailed info → Standard

Height

STAT1 · rs908598

See detailed info → Standard

Height

CD163L1 · rs79461431

See detailed info → Standard

Height (standard GWA)

HINT1 · rs79417906

See detailed info → Standard

Height

PFKFB3 · rs7916923

See detailed info → Standard

Height (standard GWA)

SPAAR · rs7861134

See detailed info → Standard

Height (standard GWA)

near Y_RNA · rs78240897

See detailed info → Standard

Height

near TMEM229A · rs7789425

See detailed info → Standard

Height

near ZNF570 · rs76943786

See detailed info → Standard

Height

LINC02042 · rs7646996

See detailed info → Standard

Height (baseline)

CHD6 · rs73611300

See detailed info → Standard

Height (baseline)

FBRSL1 · rs73486474

See detailed info → Standard

Height (baseline)

INSR · rs73002048

See detailed info → Standard

Height (baseline)

BMP6 · rs72827090

See detailed info → Standard

Height (baseline)

PTPN14 · rs72759634

See detailed info →

Showing 20 of 11491 · page 301 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.