Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5882115 1.000 0.120 7 7233965 intron variant -/C delins 7.6E-02 1
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
rs4646 0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs9138 0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
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
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs660895 0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 10
rs3803800 0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs3218977 0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs859 0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs17019602 1.000 0.120 1 107646236 intron variant A/G snv 0.19 1
rs2072392
BID
1.000 0.120 22 17743846 synonymous variant A/G snv 2.8E-02 4.1E-02 1
rs2738048 1.000 0.120 8 6965263 downstream gene variant A/G snv 0.28 1
rs4288398 1.000 0.120 8 7024116 downstream gene variant A/G snv 0.70 1
rs761991666 1.000 0.120 7 7234516 missense variant A/G snv 4.0E-06 7.0E-06 1