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: rs66468541
rs66468541
4 0.925 0.080 2 197497275 missense variant C/T snv 0.810 1.000 1 2008 2008
dbSNP: rs863224878
rs863224878
1 1.000 0.080 2 197487161 missense variant G/A snv 0.700 0