Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1021662947
rs1021662947
PALB2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1023534466
rs1023534466
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR

dbSNP: rs1025339570
rs1025339570
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1028347439
rs1028347439
BRIP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894094
rs104894094
CDKN2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894097
rs104894097
CDKN2A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs104894259
rs104894259
MEN1 ; MAP4K2
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894267
rs104894267
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR

dbSNP: rs1049900772
rs1049900772
ATM
T 0.700 CausalMutation CLINVAR

dbSNP: rs1054003194
rs1054003194
MSH6 ; FBXO11
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1054003194
rs1054003194
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516238
rs1057516238
ATM
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516291
rs1057516291
FANCC
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516668
rs1057516668
NBN
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057516772
rs1057516772
NBN
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516944
rs1057516944
ATM
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057516981
rs1057516981
ATM
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057517140
rs1057517140
ATM
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057517209
rs1057517209
NBN
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517226
rs1057517226
ATM
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517457
rs1057517457
MUTYH
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057517539
rs1057517539
PALB2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057517542
rs1057517542
CDH1
A 0.700 GeneticVariation CLINVAR