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 (baseline)

RFX4 · rs4964481

See detailed info → Standard

Height (baseline)

near ZNF101 · rs4808981

See detailed info → Standard

Height (standard GWA)

near MAU2 · rs4808948

See detailed info → Standard

Height

UHRF1 · rs4807665

See detailed info → Standard

Height (baseline)

near SNX13 · rs2537604

See detailed info → Standard

Height

HNRNPA1L3 · rs2221099

See detailed info → Standard

Height (baseline)

near LINC03007 · rs1993094

See detailed info → Standard

Height (baseline)

SCMH1 · rs17358038

See detailed info → Standard

Height

near RANBP3L · rs17284443

See detailed info → Standard

Height

CSGALNACT1 · rs17128665

See detailed info → Standard

Height

near ESR1 · rs17081542

See detailed info → Standard

Height

LYPLAL1-DT · rs17048887

See detailed info → Standard

Height (baseline)

LTBP4 · rs144879806

See detailed info → Standard

Height

CCDC73 · rs143110026

See detailed info → Standard

Height

LY6E-DT · rs12682437

See detailed info → Standard

Height (baseline)

RNF220 · rs12409669

See detailed info → Standard

Height

DMXL2 · rs11855041

See detailed info → Standard

Height (baseline)

near ATAD2 · rs116856618

See detailed info → Standard

Height (baseline)

MAP4 · rs114972739

See detailed info → Standard

Height (baseline)

USP36 · rs111544658

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Showing 20 of 11879 · page 356 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.