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 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,432 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

near CHST3 · rs16929561

See detailed info → Standard

Height

near U6 · rs16888185

See detailed info → Standard

Height

CACNA1E · rs16858051

See detailed info → Standard

Height

PI4KA · rs165818

See detailed info → Standard

Height (baseline)

CORO7-PAM16 · rs149413687

See detailed info → Standard

Height (baseline)

MORN1 · rs149229890

See detailed info → Standard

Height

RAPGEF4 · rs146346995

See detailed info → Standard

Standing height (UKB data field 50)

SMG7 · rs144712473

See detailed info → Standard

Height (baseline)

CCDC26 · rs1433576

See detailed info → Standard

Standing height (UKB data field 50)

L3MBTL3 · rs143126170

See detailed info → Standard

Height (baseline)

ENSA · rs142668571

See detailed info → Standard

Height (baseline)

near ATP5F1EP1 · rs139144061

See detailed info → Standard

Height

TESHL · rs13425869

See detailed info → Standard

Height

near RIMS1 · rs1334342

See detailed info → Standard

Height

UBAP1 · rs13302285

See detailed info → Standard

Height

LINC01505 · rs13294274

See detailed info → Standard

Height

near EEF1A1P35 · rs13144694

See detailed info → Standard

Height (baseline)

near Y_RNA · rs13120076

See detailed info → Standard

Height (baseline)

FAM169BP · rs12908109

See detailed info → Standard

Height

CASP10 · rs12693932

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.