Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501548
rs1060501548
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060501551
rs1060501551
ATM
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501570
rs1060501570
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501580
rs1060501580
ATM
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060501587
rs1060501587
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501600
rs1060501600
ATM
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060501610
rs1060501610
ATM
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1060501642
rs1060501642
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501659
rs1060501659
ATM
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060501669
rs1060501669
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501670
rs1060501670
ATM
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501676
rs1060501676
ATM
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060501677
rs1060501677
ATM
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501679
rs1060501679
ATM
AA 0.700 CausalMutation CLINVAR

dbSNP: rs1060501684
rs1060501684
ATM
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060501687
rs1060501687
ATM
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501700
rs1060501700
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501700
rs1060501700
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501701
rs1060501701
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501702
rs1060501702
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501703
rs1060501703
ATM
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501706
rs1060501706
ATM
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501707
rs1060501707
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060501711
rs1060501711
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501712
rs1060501712
A 0.700 CausalMutation CLINVAR