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

10,966 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.

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

← Back to Height

Standard

Standing height (UKB data field 50)

near TEAD1 · rs6485977

See detailed info → Standard

Height

CHASERR · rs4778052

See detailed info → Standard

Height

ADAMTSL1 · rs1341063

See detailed info → Standard

Height

C4orf51 · rs11100899

See detailed info → Standard

Height

LINC03007 · rs86

See detailed info → Standard

Height

PATJ · rs7547886

See detailed info → Standard

Height

near FGFR3P3 · rs6038400

See detailed info → Standard

Height

GLI2 · rs4848637

See detailed info → Standard

Height

near RN7SKP106 · rs4410752

See detailed info → Standard

Height

SLCO4C1 · rs3811976

See detailed info → Standard

Height

near MIR124-2HG · rs2612589

See detailed info → Standard

Height

near KLF6 · rs2129440

See detailed info → Standard

Height

JAZF1 · rs17156259

See detailed info → Standard

Height

near LINC02997 · rs12520934

See detailed info → Standard

Height

near QKI · rs12197528

See detailed info → Standard

Height

near SLC9A1 · rs12117956

See detailed info → Standard

Height (baseline)

IP6K1 · rs59512581

See detailed info → Standard

Height

MYO1A · rs4759273

See detailed info → Standard

Height

near TGIF2P1 · rs3123701

See detailed info → Standard

Height

STXBP4 · rs2787508

See detailed info →

Showing 20 of 10966 · page 162 of 549

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.