Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894855
rs104894855
GPC3
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501253
rs1060501253
WT1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131690795
rs1131690795
WT1 ; WT1-AS
G 0.700 CausalMutation CLINVAR

dbSNP: rs121907900
rs121907900
WT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121907906
rs121907906
WT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121907911
rs121907911
WT1 ; WT1-AS
T 0.700 CausalMutation CLINVAR

dbSNP: rs122453119
rs122453119
GPC3
A 0.700 CausalMutation CLINVAR

dbSNP: rs122453120
rs122453120
GPC3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1243010179
rs1243010179
CTCF
0.700 GeneticVariation UNIPROT

dbSNP: rs1553551874
rs1553551874
DIS3L2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554945033
rs1554945033
WT1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554945232
rs1554945232
WT1
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1554946500
rs1554946500
WT1 ; WT1-AS
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554946600
rs1554946600
WT1 ; WT1-AS
T 0.700 CausalMutation CLINVAR

dbSNP: rs1556297749
rs1556297749
GPC3
TGCAAG 0.700 CausalMutation CLINVAR

dbSNP: rs1565000973
rs1565000973
WT1 ; WT1-AS
G 0.700 CausalMutation CLINVAR

dbSNP: rs1565001383
rs1565001383
WT1 ; WT1-AS
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569392947
rs1569392947
GPC3
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569408743
rs1569408743
GPC3
T 0.700 CausalMutation CLINVAR

dbSNP: rs28897756
rs28897756
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507327
rs397507327
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507404
rs397507404
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397508045
rs397508045
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs41293497
rs41293497
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs41293511
rs41293511
BRCA2
C 0.700 CausalMutation CLINVAR