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: rs1468024757
rs1468024757
1 1.000 0.280 5 140676749 missense variant C/G snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs755882900
rs755882900
1 1.000 0.280 5 140677102 missense variant C/A snv 4.0E-06 0.010 1.000 1 2011 2011