Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs140490 1.000 0.080 22 21567397 intron variant G/A;C;T snv 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs200395694 1.000 0.080 1 156480799 intron variant G/A;C;T snv 2.7E-05; 1.2E-04; 1.6E-03 2
rs2066363 0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs229541 0.807 0.200 22 37195278 intron variant G/A snv 0.49 8
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs3087456 0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs34933034
CSK
0.925 0.120 15 74787133 intron variant G/A;T snv 3
rs36001488 0.724 0.240 2 233276621 intron variant C/T snv 0.44 14