Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran. 28451532

2017
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. 26226137

2016
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. 26561413

2015
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing. 24105371

2014
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss. 23770805

2013
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F. 19375528

2009
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 GeneticVariation CLINVAR Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity. 10094549

1999
dbSNP: rs747656448
rs747656448
MYO7A
A 0.700 CausalMutation CLINVAR