Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3794012 0.882 0.120 11 8248697 intron variant T/C snv 0.32 3
rs4237770 0.882 0.120 11 8254288 intron variant T/C snv 0.37 3
rs442264 0.882 0.120 11 8242602 intron variant G/A snv 0.44 3
rs138047632 0.882 0.120 21 45525860 missense variant A/G snv 2.4E-03 2.2E-03 3
rs57725551 0.882 0.120 21 45525868 synonymous variant G/T snv 5.3E-03 7.0E-03 3
rs62571442 0.882 0.120 9 134850278 non coding transcript exon variant G/A;C;T snv 0.58; 4.4E-03 3
rs414580 0.882 0.120 8 16177793 intron variant T/A;C snv 3
rs12803915 0.882 0.120 11 65444508 non coding transcript exon variant G/A snv 0.16 0.17 3
rs1482545954 0.882 0.120 19 54982407 missense variant C/T snv 7.0E-06 3
rs1194008138 0.882 0.120 5 143400121 missense variant T/C snv 4.0E-06 3
rs1361742125 0.882 0.120 5 143399842 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1412792500 0.882 0.120 5 143400541 missense variant T/C snv 4.0E-06 1.4E-05 3
rs1427331568 0.882 0.120 5 143314010 missense variant G/C snv 3
rs72481843 0.882 0.120 5 143300685 splice donor variant C/G snv 3
rs768315648 0.882 0.120 5 143399830 missense variant T/C snv 1.2E-05 3
rs772470710 0.882 0.120 4 1961074 missense variant G/A snv 4.0E-06 3
rs885822 0.882 0.120 10 70598821 missense variant G/A;C snv 0.64 3
rs6461639 0.882 0.120 7 22147337 intron variant T/A;C snv 3
rs12402181 0.882 0.120 1 66628488 mature miRNA variant G/A snv 0.17 0.24 3
rs1051296 0.882 0.120 21 45514947 3 prime UTR variant A/C snv 0.43 0.44 3
rs4149009 0.882 0.120 12 21267537 3 prime UTR variant C/T snv 0.38 3
rs2742038 0.882 0.120 10 101137330 3 prime UTR variant C/T snv 0.16 3
rs6589664 0.882 0.120 11 118534089 synonymous variant G/A snv 0.30 0.27 3
rs143125661 0.882 0.120 6 18149120 missense variant C/T snv 4.0E-06 7.0E-06 3
rs1310678797
VDR
0.882 0.120 12 47857143 missense variant C/T snv 7.0E-06 3