Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35689081
rs35689081
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		A 0.700 CausalMutation CLINVAR Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations. 19074810

2009
dbSNP: rs35689081
rs35689081
MYO7A
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		A 0.700 CausalMutation CLINVAR Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity. 10094549

1999