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: rs397507615
rs397507615
BRCA2
1 1.000 0.080 13 32319200 missense variant C/T snv 4.0E-06 0.700 1.000 20 1997 2006