USH1G, USH1 protein network component sans, 124590

N. diseases: 52; N. variants: 14
Disease: USHER SYNDROME, TYPE IG ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894652
rs104894652
Entrez Id: 92736;124590
Gene Symbol: OTOP2;USH1G
OTOP2;USH1G
CUI: C1847089
Disease:
USHER SYNDROME, TYPE IG 		T 0.700 CausalMutation CLINVAR