Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs6983561 0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs772893086 0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 9
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 27
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs61552325 0.882 0.080 17 39727784 missense variant C/G snv 5
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26