Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,452 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.

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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

Height (standard GWA)

MEPE · rs4345135

See detailed info → Standard

Height

RNF150 · rs3909595

See detailed info → Standard

Height (baseline)

MICAL3 · rs388415

See detailed info → Standard

Height (baseline)

near KRT18P64 · rs3857477

See detailed info → Standard

Height

COL6A2 · rs3810590

See detailed info → Standard

Height

ZMYND8 · rs3746483

See detailed info → Standard

Height (baseline)

IGF1R · rs3743254

See detailed info → Standard

Height (baseline)

KIF17 · rs35103949

See detailed info → Standard

Height (baseline)

near FGFR4 · rs34860731

See detailed info → Standard

Height (baseline)

COMMD4 · rs34234047

See detailed info → Standard

Height (baseline)

near LACTBL1 · rs2869052

See detailed info → Standard

Height

near LINC01419 · rs28688389

See detailed info → Standard

Height

GOT1-DT · rs2862596

See detailed info → Standard

Height (baseline)

CREB5 · rs28522092

See detailed info → Standard

Height (baseline)

SFRP4 · rs28446859

See detailed info → Standard

Height

PGM2 · rs2714555

See detailed info → Standard

Height

near RNU6ATAC32P · rs2666874

See detailed info → Standard

Height

near HMGN1P19 · rs260356

See detailed info → Standard

Height (standard GWA)

NOP14-AS1 · rs2515960

See detailed info → Standard

Height

DNM3 · rs2421994

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Showing 20 of 11452 · page 248 of 573

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.