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 2,516,056 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)

near SLC38A3 · rs557947378

See detailed info → Standard

Height

near ARRDC2 · rs388159

See detailed info → Standard

Height

TEAD1 · rs3915398

See detailed info → Standard

Height

LRMDA · rs7090265

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

DRAIC · rs77529862

See detailed info → Standard

Height

FAM98A · rs6746691

See detailed info → Standard

Height (baseline)

NCOA1 · rs17791703

See detailed info → Standard

Height

C16orf95 · rs17770752

See detailed info → Standard

Height

CATSPER3 · rs10072362

See detailed info → Standard

Height

WDR72 · rs10851543

See detailed info → Standard

Height

RNF10 · rs4102203

See detailed info → Standard

Height

ATP9A · rs2235863

See detailed info → Standard

Height

LINC01013 · rs6917644

See detailed info → Standard

Height

near LYZ · rs17813281

See detailed info → Standard

Height (baseline)

near IHH · rs138809270

See detailed info → Standard

Height

near RNU4-76P · rs10457420

See detailed info → Standard

Height

DNAAF9 · rs6051836

See detailed info → Standard

Height

PHF20L1 · rs235428

See detailed info → Standard

Height

CCDC3 · rs35859988

See detailed info → Standard

Height

FGFR3 · rs3135848

See detailed info →

Showing 20 of 11879 · page 65 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.