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: rs863225044
rs863225044
1 1.000 10 95637328 missense variant G/A snv 0.800 0
dbSNP: rs863225045
rs863225045
15 0.790 0.360 10 95637327 missense variant C/A;T snv 0.800 0
dbSNP: rs864321670
rs864321670
24 0.763 0.320 10 95633012 missense variant C/T snv 0.700 1.000 2 2015 2016