Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 12, 2026

11,879 positions on this site are linked to Height, out of 2,515,865 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

near LINC01622 · rs2784968

See detailed info → Standard

Height

near IGFBP3 · rs2453836

See detailed info → Standard

Height

FBXW11 · rs2288816

See detailed info → Standard

Height

BPIFB4 · rs2070326

See detailed info → Standard

Height (baseline)

near TUBB8P9 · rs182922458

See detailed info → Standard

Height (baseline)

near PNPT1 · rs182002616

See detailed info → Standard

Height

DPY19L3 · rs17832737

See detailed info → Standard

Height

MORC3 · rs17814116

See detailed info → Standard

Height

ABCE1 · rs17725600

See detailed info → Standard

Height

near PLSCR5 · rs16858692

See detailed info → Standard

Height (baseline)

EFHD1 · rs144363025

See detailed info → Standard

Height

near SPTLC1P2 · rs1397836

See detailed info → Standard

Height

IL17RB · rs12637033

See detailed info → Standard

Height

PPP2R5E · rs1255639

See detailed info → Standard

Height

near TPRA1 · rs12489937

See detailed info → Standard

Height (baseline)

HDLBP · rs12467671

See detailed info → Standard

Height (baseline)

ANXA2R-OT1 · rs12187928

See detailed info → Standard

Height

OTX2-AS1 · rs11851219

See detailed info → Standard

Height (baseline)

near RMI1 · rs11792821

See detailed info → Standard

Height

near RNU6-576P · rs11592542

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Showing 20 of 11879 · page 358 of 594

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.