Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516321
rs397516321
MYO7A
T 0.700 GeneticVariation CLINVAR Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss. 28472130

2017
dbSNP: rs397516321
rs397516321
MYO7A
T 0.700 GeneticVariation CLINVAR An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. 27460420

2016
dbSNP: rs397516321
rs397516321
MYO7A
T 0.700 GeneticVariation CLINVAR MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome. 25558175

2014
dbSNP: rs397516321
rs397516321
MYO7A
T 0.700 GeneticVariation CLINVAR Molecular epidemiology of Usher syndrome in Italy. 21738395

2011
dbSNP: rs397516321
rs397516321
MYO7A
T 0.700 GeneticVariation CLINVAR Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%. 16679490

2006