Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
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
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs16982520 1.000 0.040 20 59183665 intron variant A/G snv 0.14 4
rs17367504 1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2576178 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9