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

11,464 positions on this site are linked to Height, out of 2,509,249 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 (baseline)

near MIR17HG · rs17735324

See detailed info →
Standard

Height (baseline)

COL12A1 · rs17710795

See detailed info →
Standard

Height (baseline)

RPRD2 · rs17649760

See detailed info →
Standard

Height

STK38L · rs17411617

See detailed info →
Standard

Height

SANBR · rs1729659

See detailed info →
Standard

Height

GNGT1 · rs17241640

See detailed info →
Standard

Height (baseline)

ABI2 · rs17194601

See detailed info →
Standard

Height

near YBX1P1 · rs17103248

See detailed info →
Standard

Height (baseline)

C14orf39 · rs17097488

See detailed info →
Standard

Height

FAM83F · rs17001585

See detailed info →
Standard

Height

GALK2 · rs16962191

See detailed info →
Standard

Height

CUL3 · rs16866027

See detailed info →
Standard

Height

B4GALT6 · rs1667284

See detailed info →
Standard

Height

CD2AP · rs1564926

See detailed info →
Standard

Height (baseline)

DRAIC · rs1551831

See detailed info →
Standard

Height

near POGZ · rs1539493

See detailed info →
Standard

Height

near HAUS6P1 · rs1525575

See detailed info →
Standard

Height (baseline)

EFCAB13-DT · rs149457482

See detailed info →
Standard

Height (standard GWA)

LINC02895 · rs149232230

See detailed info →
Standard

Height (baseline)

near LINC02750 · rs147930958

See detailed info →

Showing 20 of 11464 · page 250 of 574

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.