Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015362 0.925 0.080 20 34150806 regulatory region variant C/T snv 0.42 3
rs1015363 1.000 0.040 20 34150529 intergenic variant G/A snv 0.69 1
rs10231520 1.000 0.040 7 20742471 intron variant C/T snv 0.29 1
rs1024708183 0.925 0.040 19 7909761 missense variant A/G snv 4
rs1034265990 0.925 0.120 9 21971123 missense variant G/A;T snv 4.4E-06 2
rs1035142 0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104894094 0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs104894095 0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 6
rs104894097 0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 8
rs104894098 0.851 0.200 9 21970982 missense variant A/T snv 5
rs104894099 0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 5
rs104894104 0.790 0.160 9 21971019 missense variant G/A;T snv 7
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894340 0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs10492396 0.925 0.080 13 32384750 non coding transcript exon variant G/A snv 4.8E-02 2
rs10515789 1.000 0.040 5 159079407 intron variant T/G snv 0.11 1
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1051849 1.000 0.040 17 37513222 3 prime UTR variant T/C snv 9.9E-02 1
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519702
KIT
1.000 0.040 4 54726020 missense variant T/C snv 2
rs1057519703
KIT
1.000 0.040 4 54727418 missense variant A/C;T snv 1
rs1057519704
KIT
0.882 0.080 4 54727425 missense variant T/A snv 3