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 11, 2026

11,659 positions on this site are linked to Height, out of 2,511,894 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

PIGV · rs34676516

See detailed info → Standard

Height

near GAPDHP72 · rs10946116

See detailed info → Standard

Height

EED · rs9971532

See detailed info → Standard

Height

LOXL4 · rs17524355

See detailed info → Standard

Height

near SNHG5 · rs1173416

See detailed info → Standard

Height

AGAP1 · rs10929146

See detailed info → Standard

Height

NKX2-1-AS1 · rs8006963

See detailed info → Standard

Height

PIBF1 · rs7996998

See detailed info → Standard

Height

CCDC91 · rs10843180

See detailed info → Standard

Height

ARID3B · rs6495116

See detailed info → Standard

Height

near MYOF · rs11597398

See detailed info → Standard

Height

SCUBE3 · rs3800388

See detailed info → Standard

Height (baseline)

near ARFGEF2 · rs13037063

See detailed info → Standard

Height

CMIP · rs17777603

See detailed info → Standard

Height

ANK3 · rs10821746

See detailed info → Standard

Height

PDE3A · rs7962446

See detailed info → Standard

Height

LINC02267 · rs6532646

See detailed info → Standard

Height

WNT9A · rs3820623

See detailed info → Standard

Height

SRPK2 · rs2299308

See detailed info → Standard

Height

near SCARB1 · rs10846720

See detailed info →

Showing 20 of 11659 · page 35 of 583

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.