Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894402
rs104894402
0.800 GeneticVariation UNIPROT

dbSNP: rs104894397
rs104894397
0.700 CausalMutation CLINVAR

dbSNP: rs1057517491
rs1057517491
0.700 GeneticVariation CLINVAR

dbSNP: rs1057517508
rs1057517508
0.700 GeneticVariation CLINVAR

dbSNP: rs371024165
rs371024165
0.700 GeneticVariation CLINVAR

dbSNP: rs398123814
rs398123814
0.700 CausalMutation CLINVAR

dbSNP: rs587783646
rs587783646
0.700 CausalMutation CLINVAR

dbSNP: rs587783647
rs587783647
0.700 CausalMutation CLINVAR

dbSNP: rs750188782
rs750188782
0.700 CausalMutation CLINVAR

dbSNP: rs104894401
rs104894401
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs104894402
rs104894402
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs104894406
rs104894406
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs104894407
rs104894407
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs104894413
rs104894413
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs28931595
rs28931595
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs80338950
rs80338950
0.800 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs1064797088
rs1064797088
0.700 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs1064797089
rs1064797089
0.700 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs1064797090
rs1064797090
0.700 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs28931593
rs28931593
0.700 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs80338949
rs80338949
0.700 CausalMutation CLINVAR Nonsyndromic Hearing Loss and Deafness, DFNA3 20301708

1993

dbSNP: rs104894402
rs104894402
0.800 CausalMutation CLINVAR Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. 9139825

1997

dbSNP: rs80338939
rs80338939
0.700 CausalMutation CLINVAR Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. 9328482

1997

dbSNP: rs80338939
rs80338939
0.700 CausalMutation CLINVAR Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. 9336442

1997

dbSNP: rs104894402
rs104894402
0.800 CausalMutation CLINVAR Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. 9856479

1998