Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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 NACA2 · rs78031430

See detailed info → Standard

Height (baseline)

LILRB2 · rs77679745

See detailed info → Standard

Height (baseline)

near RNU6-295P · rs75447677

See detailed info → Standard

Height

NBL1 · rs7523192

See detailed info → Standard

Height (baseline)

CCDC8 · rs75175362

See detailed info → Standard

Height

PRR34 · rs7510754

See detailed info → Standard

Height

near KCNC2 · rs7314533

See detailed info → Standard

Height (standard GWA)

DYM · rs72921677

See detailed info → Standard

Height

near JADRR · rs72681619

See detailed info → Standard

Height (baseline)

near U3 · rs7093041

See detailed info → Standard

Height

GALNT7-DT · rs6855544

See detailed info → Standard

Height (baseline)

TTBK2 · rs66530524

See detailed info → Standard

Height

near RNA5SP455 · rs6507549

See detailed info → Standard

Height (baseline)

MLF2 · rs6489734

See detailed info → Standard

Height (standard GWA)

near FST · rs62357775

See detailed info → Standard

Height (standard GWA)

EFCC1 · rs62265318

See detailed info → Standard

Height (standard GWA)

WDR81 · rs62090043

See detailed info → Standard

Height (baseline)

near RBL1 · rs568740796

See detailed info → Standard

Height (baseline)

near U3 · rs56052727

See detailed info → Standard

Height (standard GWA)

ZNF521 · rs56044429

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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.