Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121965081
rs121965081
MYO7A
0.800 GeneticVariation UNIPROT Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss. 28281779

2017
dbSNP: rs121965081
rs121965081
MYO7A
0.800 GeneticVariation UNIPROT Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. 9171832

1997
dbSNP: rs121965081
rs121965081
MYO7A
0.800 GeneticVariation UNIPROT The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. 9171833

1997
dbSNP: rs121965081
rs121965081
MYO7A
C 0.800 CausalMutation CLINVAR