Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs116840778
rs116840778
A 0.800 CausalMutation CLINVAR

dbSNP: rs116840778
rs116840778
0.800 GeneticVariation UNIPROT

dbSNP: rs116840786
rs116840786
0.800 GeneticVariation UNIPROT

dbSNP: rs116840786
rs116840786
T 0.800 CausalMutation CLINVAR

dbSNP: rs752298579
rs752298579
A 0.700 CausalMutation CLINVAR Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. 26805781

2016

dbSNP: rs104894080
rs104894080
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516028
rs1057516028
DMD
A 0.700 CausalMutation CLINVAR

dbSNP: rs1114167437
rs1114167437
DMD
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167439
rs1114167439
DMD
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692158
rs1131692158
A 0.700 CausalMutation CLINVAR

dbSNP: rs116840789
rs116840789
A 0.700 CausalMutation CLINVAR

dbSNP: rs116840795
rs116840795
0.700 GeneticVariation UNIPROT

dbSNP: rs1208636573
rs1208636573
T 0.700 GeneticVariation CLINVAR

dbSNP: rs137854521
rs137854521
CA 0.700 CausalMutation CLINVAR

dbSNP: rs142239530
rs142239530
T 0.700 GeneticVariation CLINVAR

dbSNP: rs143570936
rs143570936
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553521119
rs1553521119
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553846331
rs1553846331
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555452876
rs1555452876
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555606976
rs1555606976
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555735545
rs1555735545
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556880327
rs1556880327
DMD
CT 0.700 GeneticVariation CLINVAR

dbSNP: rs1556980528
rs1556980528
DMD
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1559697515
rs1559697515
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1567825175
rs1567825175
GAA
T 0.700 CausalMutation CLINVAR