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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2276109 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18