Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs722864 0.882 0.080 2 173118476 intron variant A/C;G;T snv 3
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs3756712 0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs180177042 0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs8042059 0.882 0.080 15 78615517 intron variant A/C;T snv 6
rs10213865 0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs12901682 0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 4
rs1397529 0.882 0.080 4 143471009 3 prime UTR variant A/C;T snv 4
rs12050604 0.882 0.080 15 43065208 intron variant A/C;T snv 3
rs3015993 0.882 0.080 11 77467875 intron variant A/C;T snv 3
rs3866958 0.882 0.080 17 19377693 intron variant A/C;T snv 0.89 3
rs4262299 0.882 0.080 8 107330035 intron variant A/C;T snv 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101