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
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9