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: rs74315450
rs74315450
5 0.851 0.120 21 34859485 missense variant C/T snv 0.020 1.000 2 2012 2015
dbSNP: rs1482518887
rs1482518887
8 0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs754894156
rs754894156
2 0.925 0.040 21 34834544 missense variant C/T snv 4.0E-06 0.010 1.000 1 2012 2012