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

11,015 positions on this site are linked to Height, out of 2,505,913 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

near LINC01478 · rs16978104

See detailed info →
Standard

Height

MICOS10-NBL1 · rs10489858

See detailed info →
Standard

Height

CHCHD7 · rs9650315

See detailed info →
Standard

Height

ZNF451 · rs9367711

See detailed info →
Standard

Height

CNN2 · rs7253254

See detailed info →
Standard

Height

ADAMTS2 · rs6881016

See detailed info →
Standard

Height

ATXN1 · rs570917

See detailed info →
Standard

Height

LINC01118 · rs4953418

See detailed info →
Standard

Height

DDB1 · rs4939513

See detailed info →
Standard

Height

PRKCA · rs17759410

See detailed info →
Standard

Height

SUPT3H · rs12530016

See detailed info →
Standard

Height

SH3PXD2A · rs10748848

See detailed info →
Standard

Height

near STMN1P2 · rs10434086

See detailed info →
Standard

Height

LINC01752 · rs6077888

See detailed info →
Standard

Height

near YWHAQ · rs13422487

See detailed info →
Standard

Height

CSMD1 · rs1038063

See detailed info →
Standard

Height

CRACD · rs2412721

See detailed info →
Standard

Height (baseline)

ADAMTSL3 · rs56278218

See detailed info →
Standard

Height

MLF2 · rs1997510

See detailed info →
Standard

Height

PALS2 · rs985062

See detailed info →

Showing 20 of 11015 · page 164 of 551

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.