Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs125701 0.790 0.160 3 9748794 upstream gene variant G/A snv 0.13 7
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2976392
JRK ; PSCA
0.724 0.240 8 142681514 3 prime UTR variant G/A snv 0.46 0.45 15
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs35592567 0.827 0.160 3 189896847 3 prime UTR variant C/G;T snv 6
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs3810366 0.732 0.280 19 45370684 5 prime UTR variant G/C;T snv 12
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs11671784 0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 9
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25