Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs10937405 0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs12203582 0.827 0.120 6 52240759 intron variant G/A;T snv 7
rs17757541 0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs6465657 0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 7
rs2168351 0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs2835267 0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs3784730 0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs2070803 0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs3114020 0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs3787728 0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs112290073 0.882 0.080 5 1285917 intron variant G/A snv 7.8E-03 4
rs1347093 0.882 0.080 2 56019205 intron variant G/T snv 0.21 4
rs138895564 0.882 0.080 5 1271959 intron variant C/T snv 5.1E-03 4