Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs371086981
rs371086981
G 0.700 GeneticVariation CLINVAR Asymmetric configurations and N-terminal rearrangements in connexin26 gap junction channels. 21094651

2011

dbSNP: rs371086981
rs371086981
G 0.700 GeneticVariation CLINVAR Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression. 12189493

2002