Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12946454 0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs2053044 1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs41511344 0.882 0.040 4 148152550 stop gained G/A;T snv 5
rs1126742 0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 4
rs1199475313 0.851 0.040 8 37966277 missense variant T/C snv 7.0E-06 4
rs1065297 0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02 3
rs12140311 1.000 0.040 1 16052230 missense variant A/C;T snv 8.0E-06; 9.6E-02 3
rs12695895 0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs13306560 1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02 3
rs13306673 1.000 0.040 16 56867019 intron variant C/T snv 0.10 0.13 3
rs2280275 0.925 0.040 1 59901568 intron variant T/C snv 0.23 3
rs2288774 1.000 0.040 18 58316098 intron variant T/A;C snv 3
rs2304595 1.000 0.040 4 186251126 non coding transcript exon variant G/A snv 0.36 3
rs3802230 1.000 0.040 8 142911448 3 prime UTR variant C/A snv 0.63 3
rs3890011 0.925 0.040 1 46933071 intron variant G/C snv 0.71 0.65 3
rs56204867 0.925 0.040 X 129656490 upstream gene variant A/G snv 0.11 3
rs10501367 1.000 0.040 11 57238113 upstream gene variant T/C snv 0.73 2
rs10803414 1.000 0.040 1 16054087 intron variant C/T snv 0.40 2
rs1093538 1.000 0.040 15 29326124 intron variant C/T snv 0.12 2
rs11685424 0.925 0.040 2 102310521 upstream gene variant G/A snv 0.54 2
rs1212768461 1.000 0.040 9 132897292 missense variant T/A;C snv 1.4E-05 2
rs121918359 0.925 0.040 13 36872722 stop gained G/A;T snv 2.4E-05 2
rs1320206988 1.000 0.040 9 132910585 missense variant T/A snv 2
rs16849802 1.000 0.040 1 163145396 3 prime UTR variant G/A snv 4.4E-03 2
rs1934953 1.000 0.040 10 95037713 intron variant C/A;T snv 2