UMOD, uromodulin, 7369

N. diseases: 164; N. variants: 35
Disease: Velopharyngeal dysfunction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12922822
rs12922822
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C4280669
Disease:
Velopharyngeal dysfunction 		0.700 GeneticVariation GWASCAT GWAS reveals loci associated with velopharyngeal dysfunction. 29855589 2018