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: rs81002831
rs81002831
BRCA2
4 0.882 0.200 13 32330918 splice acceptor variant G/C;T snv 0.700 0