Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs3212948 0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306