Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853185
rs137853185
ANAPC15 ; LRTOMT
CUI: C1969621
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 63
DEAFNESS, AUTOSOMAL RECESSIVE 63 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137853186
rs137853186
ANAPC15 ; LRTOMT
CUI: C1969621
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 63
DEAFNESS, AUTOSOMAL RECESSIVE 63 		C 0.800 CausalMutation CLINVAR

dbSNP: rs137853187
rs137853187
ANAPC15 ; LRTOMT
CUI: C1969621
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 63
DEAFNESS, AUTOSOMAL RECESSIVE 63 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137853188
rs137853188
ANAPC15 ; LRTOMT
CUI: C1969621
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 63
DEAFNESS, AUTOSOMAL RECESSIVE 63 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1565331646
rs1565331646
ANAPC15 ; LRTOMT
CUI: C1384666
Disease: hearing impairment
hearing impairment 		AGCTC 0.700 GeneticVariation CLINVAR

dbSNP: rs1565331646
rs1565331646
ANAPC15 ; LRTOMT
CUI: C1969621
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 63
DEAFNESS, AUTOSOMAL RECESSIVE 63 		AGCTC 0.700 GeneticVariation CLINVAR

dbSNP: rs545947177
rs545947177
ANAPC15 ; LRTOMT
CUI: C1969621
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 63
DEAFNESS, AUTOSOMAL RECESSIVE 63 		C 0.700 CausalMutation CLINVAR