Gene: MYO7A ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs782252317
rs782252317
MYO7A
A 0.800 GeneticVariation CLINVAR Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis. 25575603

2015
dbSNP: rs782252317
rs782252317
MYO7A
0.800 GeneticVariation UNIPROT Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients. 25798947

2015
dbSNP: rs111033178
rs111033178
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs111033181
rs111033181
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs111033181
rs111033181
MYO7A
A 0.800 GeneticVariation CLINVAR Targeted exon sequencing in Usher syndrome type I. 25468891

2014
dbSNP: rs111033181
rs111033181
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs111033206
rs111033206
MYO7A
A 0.800 GeneticVariation CLINVAR Targeted exon sequencing in Usher syndrome type I. 25468891

2014
dbSNP: rs111033206
rs111033206
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs111033206
rs111033206
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs111033214
rs111033214
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs111033214
rs111033214
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs111033215
rs111033215
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs111033283
rs111033283
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs1472566324
rs1472566324
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs1555067667
rs1555067667
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs1555067667
rs1555067667
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs199606180
rs199606180
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs199606180
rs199606180
MYO7A
T 0.800 GeneticVariation CLINVAR Targeted exon sequencing in Usher syndrome type I. 25468891

2014
dbSNP: rs199606180
rs199606180
MYO7A
T 0.800 GeneticVariation CLINVAR Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A. 24194196

2014
dbSNP: rs28934610
rs28934610
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs28934610
rs28934610
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs368657015
rs368657015
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014
dbSNP: rs397516321
rs397516321
MYO7A
0.800 GeneticVariation UNIPROT American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. 24651602

2014
dbSNP: rs397516321
rs397516321
MYO7A
T 0.800 GeneticVariation CLINVAR MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome. 25558175

2014
dbSNP: rs397516321
rs397516321
MYO7A
0.800 GeneticVariation UNIPROT Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. 24831256

2014