Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129891 0.851 0.160 6 32447303 downstream gene variant G/A snv 0.20 5
rs1881457 0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs224222 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs806378 1.000 0.040 6 88149832 intron variant C/T snv 0.21 2
rs10474485 1.000 0.040 5 76975028 intron variant C/A snv 0.26 2
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs684302 1.000 0.040 11 18038806 intron variant C/T snv 0.36 1
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs7130929 1.000 0.040 11 18046616 upstream gene variant C/A snv 0.40 1
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7209436 0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs242924 0.882 0.080 17 45808001 intron variant G/T snv 0.44 3
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs11554825 0.882 0.120 2 218261086 5 prime UTR variant C/T snv 0.44 3
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3779250 0.925 0.080 7 30654644 intron variant C/T snv 0.48 2
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs11190140 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs4722999 0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6478108 0.763 0.200 9 114796423 intron variant C/T snv 0.73 10