Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs372949028
rs372949028
A 0.700 CausalMutation CLINVAR Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. 26805781

2016

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: rs122445108
rs122445108
A 0.700 CausalMutation CLINVAR

dbSNP: rs122455132
rs122455132
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555050158
rs1555050158
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555050165
rs1555050165
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555050171
rs1555050171
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555050174
rs1555050174
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555455456
rs1555455456
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555661648
rs1555661648
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555910048
rs1555910048
TGGCCGTGGGCAGCCCC 0.700 CausalMutation CLINVAR

dbSNP: rs1562928193
rs1562928193
GAT 0.700 GeneticVariation CLINVAR

dbSNP: rs1569146649
rs1569146649
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1569161831
rs1569161831
A 0.700 GeneticVariation CLINVAR

dbSNP: rs28935468
rs28935468
A 0.700 CausalMutation CLINVAR

dbSNP: rs397515486
rs397515486
A 0.700 CausalMutation CLINVAR

dbSNP: rs398123561
rs398123561
A 0.700 CausalMutation CLINVAR

dbSNP: rs61748421
rs61748421
A 0.700 CausalMutation CLINVAR

dbSNP: rs724159949
rs724159949
T 0.700 CausalMutation CLINVAR

dbSNP: rs724159950
rs724159950
GAA 0.700 CausalMutation CLINVAR

dbSNP: rs765556214
rs765556214
C 0.700 GeneticVariation CLINVAR

dbSNP: rs794729221
rs794729221
A 0.700 CausalMutation CLINVAR

dbSNP: rs796053290
rs796053290
C 0.700 CausalMutation CLINVAR

dbSNP: rs869025287
rs869025287
T 0.700 CausalMutation CLINVAR

dbSNP: rs869312674
rs869312674
A 0.700 CausalMutation CLINVAR