Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554919471
rs1554919471
C 0.700 CausalMutation CLINVAR Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome. 29372044

2018

dbSNP: rs1057517966
rs1057517966
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518826
rs1057518826
T 0.700 GeneticVariation CLINVAR

dbSNP: rs111033334
rs111033334
A 0.700 CausalMutation CLINVAR

dbSNP: rs111033364
rs111033364
T 0.700 CausalMutation CLINVAR

dbSNP: rs199679165
rs199679165
A 0.700 CausalMutation CLINVAR

dbSNP: rs201650281
rs201650281
A 0.700 CausalMutation CLINVAR

dbSNP: rs201866631
rs201866631
A 0.700 CausalMutation CLINVAR

dbSNP: rs571007078
rs571007078
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727504301
rs727504301
A 0.700 CausalMutation CLINVAR

dbSNP: rs768257384
rs768257384
T 0.700 GeneticVariation CLINVAR

dbSNP: rs772410450
rs772410450
C 0.700 CausalMutation CLINVAR

dbSNP: rs780170125
rs780170125
T 0.700 CausalMutation CLINVAR

dbSNP: rs796052243
rs796052243
T 0.700 GeneticVariation CLINVAR

dbSNP: rs80338903
rs80338903
T 0.700 CausalMutation CLINVAR

dbSNP: rs876657731
rs876657731
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906930
rs387906930
0.010 GeneticVariation BEFREE Their father has congenital sensorineural hearing loss and developed optic atrophy.He is heterozygous for A684V in WFS1. 21067485

2010