Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1560395607
rs1560395607
KIT
C 0.700 CausalMutation CLINVAR

dbSNP: rs1560417385
rs1560417385
KIT
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417396
rs1560417396
KIT
AA 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417427
rs1560417427
KIT
CC 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417438
rs1560417438
KIT
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417535
rs1560417535
KIT
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417642
rs1560417642
KIT
GACCCAACACAACTTCCTTATGATCACAAATGGGAGTTTCCCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417666
rs1560417666
KIT
ACACAACTTCCTTATGATCACAAATGGGAGTTTCCCAGAAACAGGC 0.700 GeneticVariation CLINVAR

dbSNP: rs1560417673
rs1560417673
KIT
CACAACTTCCTTATGATCACAAATGGGAGTTTCCCAGAAACAGGCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1560420761
rs1560420761
KIT
T 0.700 CausalMutation CLINVAR

dbSNP: rs267606600
rs267606600
NF1
C 0.700 CausalMutation CLINVAR

dbSNP: rs587776653
rs587776653
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776793
rs587776793
G 0.700 CausalMutation CLINVAR

dbSNP: rs587776794
rs587776794
GGAGGGA 0.700 CausalMutation CLINVAR

dbSNP: rs587776795
rs587776795
G 0.700 CausalMutation CLINVAR

dbSNP: rs587776804
rs587776804
KIT
A 0.700 CausalMutation CLINVAR

dbSNP: rs587782617
rs587782617
T 0.700 CausalMutation CLINVAR

dbSNP: rs606231209
rs606231209
C 0.700 CausalMutation CLINVAR

dbSNP: rs74315367
rs74315367
C 0.700 GeneticVariation CLINVAR

dbSNP: rs74315369
rs74315369
A 0.700 CausalMutation CLINVAR

dbSNP: rs747518441
rs747518441
T 0.700 GeneticVariation CLINVAR

dbSNP: rs786202732
rs786202732
G 0.700 CausalMutation CLINVAR

dbSNP: rs786203506
rs786203506
C 0.700 CausalMutation CLINVAR

dbSNP: rs794728947
rs794728947
TG 0.700 CausalMutation CLINVAR

dbSNP: rs869025568
rs869025568
KIT
C 0.700 GeneticVariation CLINVAR