Gene: BRCA2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28897759
rs28897759
BRCA2
T 0.810 GeneticVariation CLINVAR

dbSNP: rs28897759
rs28897759
BRCA2
0.810 GeneticVariation UNIPROT

dbSNP: rs41293511
rs41293511
BRCA2
C 0.800 CausalMutation CLINVAR

dbSNP: rs45580035
rs45580035
BRCA2
T 0.800 CausalMutation CLINVAR

dbSNP: rs80359014
rs80359014
BRCA2
T 0.800 CausalMutation CLINVAR

dbSNP: rs80359014
rs80359014
BRCA2
0.800 GeneticVariation UNIPROT

dbSNP: rs80359065
rs80359065
BRCA2
0.730 GeneticVariation UNIPROT

dbSNP: rs28897743
rs28897743
BRCA2
C 0.710 CausalMutation CLINVAR

dbSNP: rs28897743
rs28897743
BRCA2
A 0.710 CausalMutation CLINVAR

dbSNP: rs80358807
rs80358807
BRCA2
T 0.710 CausalMutation CLINVAR

dbSNP: rs80359078
rs80359078
BRCA2
0.710 GeneticVariation UNIPROT

dbSNP: rs80359182
rs80359182
BRCA2
0.710 GeneticVariation UNIPROT

dbSNP: rs80359198
rs80359198
BRCA2
0.710 GeneticVariation UNIPROT

dbSNP: rs1135401927
rs1135401927
BRCA2
TA 0.700 CausalMutation CLINVAR

dbSNP: rs11571747
rs11571747
BRCA2
0.700 GeneticVariation UNIPROT

dbSNP: rs11571769
rs11571769
BRCA2
0.700 GeneticVariation UNIPROT

dbSNP: rs1298550035
rs1298550035
BRCA2
0.700 GeneticVariation UNIPROT

dbSNP: rs1555281715
rs1555281715
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555283256
rs1555283256
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555287766
rs1555287766
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs276174853
rs276174853
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs276174900
rs276174900
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs28897706
rs28897706
BRCA2
0.700 GeneticVariation UNIPROT

dbSNP: rs28897708
rs28897708
BRCA2
0.700 GeneticVariation UNIPROT

dbSNP: rs28897751
rs28897751
BRCA2
0.700 GeneticVariation UNIPROT