Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1338605788
rs1338605788
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1386887007
rs1386887007
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1555076948
rs1555076948
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1565402473
rs1565402473
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1565455391
rs1565455391
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR

dbSNP: rs750358148
rs750358148
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		G 0.700 CausalMutation CLINVAR

dbSNP: rs781989117
rs781989117
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs782255281
rs782255281
MYO7A
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR