Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1374999656
rs1374999656
SLC26A4
A 0.700 CausalMutation CLINVAR Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: a new approach for newborn screening follow-up. 16950989

2006
dbSNP: rs1374999656
rs1374999656
SLC26A4
A 0.700 CausalMutation CLINVAR Two frequent missense mutations in Pendred syndrome. 9618166

1998