Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1269396908
rs1269396908
ESRRB
0.010 GeneticVariation BEFREE The known pathogenic c.226C>T variant identified in <i>KCNE1</i> only segregates with the hearing loss phenotype in a subset of affected members of the family GCNF21. 31835641

2019