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: rs111033615
rs111033615
F8
1 1.000 0.080 X 154904004 missense variant C/T snv 0.810 1.000 23 1989 2013