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

11,083 positions on this site are linked to Height, out of 2,506,337 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 KRTAP21-1 · rs2833084

See detailed info → Standard

Height

LRRC8D · rs2802031

See detailed info → Standard

Height

near RPSAP20 · rs2793677

See detailed info → Standard

Height

MAP2K6 · rs2716195

See detailed info → Standard

Height (baseline)

PVT1 · rs2608037

See detailed info → Standard

Height

near TSPYL5 · rs2583503

See detailed info → Standard

Height

USP25 · rs2026853

See detailed info → Standard

Height

KIN · rs2026612

See detailed info → Standard

Height

KCNQ3 · rs1962131

See detailed info → Standard

Height

CAMK1D · rs1929383

See detailed info → Standard

Height

FGD6 · rs2043368

See detailed info → Standard

Standing height (UKB data field 50)

CERS2 · rs185823447

See detailed info → Standard

Height (baseline)

near UBE2Q2P8 · rs182029683

See detailed info → Standard

Height (baseline)

FBN2 · rs17676694

See detailed info → Standard

Standing height (UKB data field 50)

ST8SIA1 · rs17646466

See detailed info → Standard

Height (baseline)

ACAN · rs17200595

See detailed info → Standard

Height

ATP2B2 · rs17032981

See detailed info → Standard

Height

LINC00506 · rs17023802

See detailed info → Standard

Height

near RAI14-DT · rs16903378

See detailed info → Standard

Height

KPNA6 · rs16834897

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.