Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204739
rs786204739
SLC26A4
G 0.700 GeneticVariation CLINVAR Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China. 28786104

2017
dbSNP: rs786204739
rs786204739
SLC26A4
G 0.700 GeneticVariation CLINVAR A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China. 17718863

2007
dbSNP: rs786204739
rs786204739
SLC26A4
G 0.700 CausalMutation CLINVAR