Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012477 0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1042489 0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1394960893 0.807 0.240 11 67586553 synonymous variant C/T snv 6
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16917496 0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2279115 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2645429 0.790 0.120 8 11802542 non coding transcript exon variant A/G;T snv 7
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65