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.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Height (standard GWA)

DELEC1 · rs62578006

See detailed info → Standard

Height

near SNAI1 · rs6091084

See detailed info → Standard

Height (baseline)

near FUNDC2P4 · rs60044379

See detailed info → Standard

Height

near MRPS18CP4 · rs58612760

See detailed info → Standard

Height

near SLC6A12 · rs478455

See detailed info → Standard

Height

near RPS27P16 · rs4722974

See detailed info → Standard

Height

near PPIAP80 · rs4722780

See detailed info → Standard

Height

near WNT4 · rs4654783

See detailed info → Standard

Height

near LINC02307 · rs4551953

See detailed info → Standard

Height (baseline)

near U8 · rs4515014

See detailed info → Standard

Height (baseline)

CALB2 · rs4412976

See detailed info → Standard

Height (baseline)

RNLS · rs3781201

See detailed info → Standard

Height

near COPS7B · rs374935766

See detailed info → Standard

Height

VPS36 · rs35794740

See detailed info → Standard

Height (baseline)

C15orf39 · rs34838371

See detailed info → Standard

Height

ANKDD1B · rs34355

See detailed info → Standard

Height (baseline)

RASGEF1C · rs34351120

See detailed info → Standard

Height

HCG20 · rs3131036

See detailed info → Standard

Height

near B4GALT5 · rs3091975

See detailed info → Standard

Height (baseline)

ERC1 · rs2968877

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.