Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205155
rs786205155
ETV6
C 0.710 CausalMutation CLINVAR

dbSNP: rs879255268
rs879255268
SRC
A 0.710 GeneticVariation CLINVAR

dbSNP: rs1064797085
rs1064797085
FLI1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs138924661
rs138924661
TRIM25 ; DGKE
A 0.700 CausalMutation CLINVAR

dbSNP: rs1441937959
rs1441937959
EFL1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553196096
rs1553196096
CDC42
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554162524
rs1554162524
ELOVL4
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554785242
rs1554785242
ADAMTS13
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554791280
rs1554791280
ADAMTS13
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554800065
rs1554800065
ANKRD26
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1556620697
rs1556620697
SH2D1A ; STAG2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1569061762
rs1569061762
RUNX1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569061768
rs1569061768
RUNX1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs190521996
rs190521996
PMM2
C 0.700 CausalMutation CLINVAR

dbSNP: rs397518423
rs397518423
PIK3CD
A 0.700 CausalMutation CLINVAR

dbSNP: rs555607708
rs555607708
CHEK2
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776456
rs587776456
GATA1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs757788894
rs757788894
CLCN7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs786205154
rs786205154
ETV6
A 0.700 CausalMutation CLINVAR

dbSNP: rs80338701
rs80338701
PMM2
A 0.700 CausalMutation CLINVAR

dbSNP: rs867593888
rs867593888
MYH9
C 0.700 GeneticVariation CLINVAR

dbSNP: rs869320714
rs869320714
SLFN14
T 0.700 GeneticVariation CLINVAR

dbSNP: rs869320715
rs869320715
SLFN14
A 0.700 GeneticVariation CLINVAR

dbSNP: rs878853314
rs878853314
GBA
G 0.700 GeneticVariation CLINVAR

dbSNP: rs878853315
rs878853315
GBA
C 0.700 GeneticVariation CLINVAR