Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs128620185
rs128620185
BTK
T 0.810 CausalMutation CLINVAR

dbSNP: rs128620189
rs128620189
BTK
G 0.810 CausalMutation CLINVAR

dbSNP: rs128621190
rs128621190
BTK
T 0.810 CausalMutation CLINVAR

dbSNP: rs104894770
rs104894770
BTK
G 0.800 CausalMutation CLINVAR

dbSNP: rs128620183
rs128620183
BTK
T 0.800 CausalMutation CLINVAR

dbSNP: rs128620184
rs128620184
BTK
C 0.800 CausalMutation CLINVAR

dbSNP: rs128621194
rs128621194
BTK
A 0.800 CausalMutation CLINVAR

dbSNP: rs128621194
rs128621194
BTK
A 0.800 GeneticVariation CLINVAR

dbSNP: rs128621195
rs128621195
BTK
C 0.800 CausalMutation CLINVAR

dbSNP: rs128621196
rs128621196
BTK
G 0.800 CausalMutation CLINVAR

dbSNP: rs128621198
rs128621198
BTK
G 0.800 CausalMutation CLINVAR

dbSNP: rs128621200
rs128621200
BTK
G 0.800 CausalMutation CLINVAR

dbSNP: rs128621202
rs128621202
BTK
T 0.800 CausalMutation CLINVAR

dbSNP: rs128621204
rs128621204
BTK
A 0.800 CausalMutation CLINVAR

dbSNP: rs128621205
rs128621205
BTK
G 0.800 CausalMutation CLINVAR

dbSNP: rs128621206
rs128621206
BTK
C 0.800 CausalMutation CLINVAR

dbSNP: rs128621208
rs128621208
BTK
T 0.800 CausalMutation CLINVAR

dbSNP: rs128621209
rs128621209
BTK
T 0.800 CausalMutation CLINVAR

dbSNP: rs128622212
rs128622212
G 0.800 CausalMutation CLINVAR

dbSNP: rs28935478
rs28935478
BTK
C 0.800 CausalMutation CLINVAR

dbSNP: rs41310709
rs41310709
BTK
T 0.800 CausalMutation CLINVAR

dbSNP: rs1131691354
rs1131691354
BTK
T 0.700 CausalMutation CLINVAR

dbSNP: rs128620186
rs128620186
BTK
G 0.700 CausalMutation CLINVAR

dbSNP: rs128620187
rs128620187
BTK
A 0.700 CausalMutation CLINVAR

dbSNP: rs128620188
rs128620188
BTK
A 0.700 CausalMutation CLINVAR