Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs9282858 0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16