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 9, 2026

11,449 positions on this site are linked to Height, out of 2,509,139 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

Height (baseline)

MOB3B · rs62541572

See detailed info → Standard

Height

near HCN1 · rs62369904

See detailed info → Standard

Height (baseline)

near CHD6 · rs62208546

See detailed info → Standard

Height (baseline)

near PAIP2B · rs62143414

See detailed info → Standard

Height

near ZBTB7A · rs62131558

See detailed info → Standard

Height (baseline)

near XAF1 · rs62063978

See detailed info → Standard

Height (baseline)

KIF7 · rs62021460

See detailed info → Standard

Height (baseline)

PTPN14 · rs61819644

See detailed info → Standard

Height (baseline)

DNASE1L3 · rs61072144

See detailed info → Standard

Height

near LINC01728 · rs6073238

See detailed info → Standard

Height (baseline)

MANSC1 · rs57725255

See detailed info → Standard

Height (baseline)

near PDGFB · rs5757602

See detailed info → Standard

Height (baseline)

near PREX1 · rs56256142

See detailed info → Standard

Height (baseline)

CCDC3 · rs55895916

See detailed info → Standard

Height (baseline)

near HLA-DQA1 · rs555548512

See detailed info → Standard

Height (baseline)

near OR5C1 · rs542119549

See detailed info → Standard

Height (baseline)

ACAN · rs4932434

See detailed info → Standard

Height (baseline)

near U6 · rs481012

See detailed info → Standard

Height (baseline)

near XYLT1 · rs4781974

See detailed info → Standard

Height (standard GWA)

BOC · rs4682132

See detailed info →

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.