Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs80356880
rs80356880
BRCA1
5 0.851 0.080 17 43115750 missense variant G/C;T snv 0.700 0
dbSNP: rs879255498
rs879255498
BRCA1
4 0.851 0.080 17 43094606 stop gained T/A;C snv 0.700 0
dbSNP: rs80357382
rs80357382
BRCA1
11 0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 0.700 0