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
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29