Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs6062302 0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 4
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1642785 0.807 0.200 17 7676483 5 prime UTR variant G/A;C;T snv 1.2E-05; 0.67; 2.8E-05 6
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2239647 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs1052576 0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2235573 0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs643788 1.000 0.040 11 119097048 missense variant T/C snv 0.42 0.38 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs5019252 1.000 0.040 20 63746996 synonymous variant C/T snv 0.34 0.30 1
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs34988193 1.000 0.040 15 64943580 missense variant A/G snv 0.31 0.28 2