MEOX2, mesenchyme homeobox 2, 4223

N. diseases: 29; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6980299
rs6980299
Entrez Id: 4223;105375166
Gene Symbol: MEOX2;LOC105375166
MEOX2;LOC105375166
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019