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: rs104894159
rs104894159
5 0.827 0.080 10 62813413 missense variant G/A snv 0.800 1.000 7 1998 2005
dbSNP: rs104894161
rs104894161
6 0.807 0.080 10 62813563 missense variant G/A snv 0.800 1.000 7 1998 2005
dbSNP: rs104894160
rs104894160
2 0.925 0.080 10 62813491 missense variant C/A snv 0.700 1.000 7 1998 2005
dbSNP: rs281865137
rs281865137
4 0.851 0.080 10 62813496 missense variant C/T snv 0.700 1.000 7 1998 2005