Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs2306283 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs1256046734 0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs267606661 0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs717620 0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs198389 0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs694539 0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs764929617 0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs3816873 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs573658040 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs2228314 0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs4973768 0.807 0.120 3 27374522 3 prime UTR variant C/T snv 0.44 7