Gene Knowledge Graph

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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

11,696 positions on this site are linked to Height, out of 2,512,461 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

Standing height (UKB data field 50)

UQCC6 · rs11616083

See detailed info → Standard

Height (baseline)

near INSYN1-AS1 · rs716828

See detailed info → Standard

Height

near LINC01713 · rs6054484

See detailed info → Standard

Height

PARP12 · rs2286198

See detailed info → Standard

Height (baseline)

near RN7SL323P · rs145846214

See detailed info → Standard

Height

PALM2AKAP2 · rs7855586

See detailed info → Standard

Height (baseline)

ARNILA · rs35800274

See detailed info → Standard

Height (standard GWA)

ADAMTS19 · rs1363146

See detailed info → Standard

Standing height (UKB data field 50)

near LINC01635 · rs12730256

See detailed info → Standard

Height

CTSH · rs12148472

See detailed info → Standard

Height (baseline)

STRADA · rs145751091

See detailed info → Standard

Standing height (UKB data field 50)

near Y_RNA · rs7031032

See detailed info → Standard

Height (baseline)

near HLA-DQB1 · rs554448117

See detailed info → Standard

Height (baseline)

near BPIFB5P · rs117824493

See detailed info → Standard

Height (baseline)

near RPL17P16 · rs75354213

See detailed info → Standard

Height

near INSR · rs7507911

See detailed info → Standard

Height (baseline)

ZNF341 · rs73622547

See detailed info → Standard

Height (baseline)

DNM3 · rs631154

See detailed info → Standard

Height

BNC2 · rs4961737

See detailed info → Standard

Height

near CCDC6 · rs3763745

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.