Gene: BRCA2 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135401927
rs1135401927
BRCA2
TA 0.700 CausalMutation CLINVAR

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: rs28897756
rs28897756
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507327
rs397507327
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507389
rs397507389
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507404
rs397507404
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507411
rs397507411
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507419
rs397507419
BRCA2
CA 0.700 CausalMutation CLINVAR

dbSNP: rs397507586
rs397507586
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507637
rs397507637
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507787
rs397507787
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397508045
rs397508045
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397508058
rs397508058
BRCA2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397515636
rs397515636
BRCA2
CTGCT 0.700 CausalMutation CLINVAR

dbSNP: rs41293497
rs41293497
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs587776351
rs587776351
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs587779358
rs587779358
BRCA2
TTT 0.700 CausalMutation CLINVAR

dbSNP: rs587779363
rs587779363
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs587779364
rs587779364
BRCA2
TC 0.700 CausalMutation CLINVAR

dbSNP: rs587781629
rs587781629
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs690016538
rs690016538
BRCA2
CA 0.700 CausalMutation CLINVAR