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: rs778212685
rs778212685
8 0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs786203472
rs786203472
5 0.827 0.120 22 28719414 start lost T/C snv 0.010 1.000 1 2004 2004
dbSNP: rs863224748
rs863224748
5 0.827 0.120 22 28734721 start lost T/C snv 0.010 1.000 1 2004 2004