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

11,486 positions on this site are linked to Height, out of 2,509,513 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

Standard

Height (baseline)

ADAMTS17 · rs117672071

See detailed info →
Standard

Height

TMEM178B · rs11764939

See detailed info →
Standard

Height (baseline)

SLC38A4-AS1 · rs117498071

See detailed info →
Standard

Height

TMEM67 · rs117488621

See detailed info →
Standard

Height

ABCC1 · rs11647513

See detailed info →
Standard

Height (baseline)

CBFA2T3 · rs11646968

See detailed info →
Standard

Height (baseline)

ANTXR1 · rs116024256

See detailed info →
Standard

Height (baseline)

near RNA5SP142 · rs115945771

See detailed info →
Standard

Height

CWC27 · rs1159105

See detailed info →
Standard

Height (standard GWA)

ATIC · rs115313843

See detailed info →
Standard

Height (baseline)

VEPH1 · rs115072820

See detailed info →
Standard

Height (baseline)

LCORL · rs114542905

See detailed info →
Standard

Height

PDE4B · rs11208834

See detailed info →
Standard

Height (baseline)

near PPP1R3C · rs11186639

See detailed info →
Standard

Height (standard GWA)

FRK · rs11153591

See detailed info →
Standard

Height

ANKS1B · rs11109986

See detailed info →
Standard

Height

CRADD · rs11107175

See detailed info →
Standard

Height

near LINC01132 · rs10910490

See detailed info →
Standard

Height (standard GWA)

near FUBP3 · rs10793939

See detailed info →
Standard

Height (baseline)

near KCNJ2 · rs10512537

See detailed info →

Showing 20 of 11486 · page 277 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.