Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs1064794312 0.925 0.080 17 7674278 missense variant A/G snv 8.0E-06 2
rs1064795369 0.882 0.080 17 7673791 missense variant A/C;G snv 3
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691036 0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs1159579789 0.925 0.080 17 7673578 missense variant T/C snv 4.0E-06 3
rs1177881399 0.925 0.080 17 7673557 missense variant T/C snv 4.0E-06 2
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs1237722021 0.925 0.080 17 7676194 missense variant C/A snv 7.0E-06 2
rs1288373809 0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs1457582183 0.827 0.200 17 7673608 missense variant G/A;C snv 7.0E-06 5
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs1800372 0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs2287499 0.925 0.080 17 7688850 missense variant C/G;T snv 0.20 4
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47