Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3916966 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 4
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs7452939 0.882 0.080 6 132572626 downstream gene variant G/A snv 4
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1935062 0.882 0.080 13 105475787 intron variant A/C snv 0.32 3
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1409851868 0.882 0.080 3 89399325 missense variant A/G snv 6
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174