Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111978267 0.882 0.120 11 2751648 intron variant C/G;T snv 2.8E-05 3
rs1169704167
ATM
0.882 0.120 11 108284370 frameshift variant -/T delins 8.0E-06 3
rs1194008138 0.882 0.120 5 143400121 missense variant T/C snv 4.0E-06 3
rs12402181 0.882 0.120 1 66628488 mature miRNA variant G/A snv 0.17 0.24 3
rs12434881 0.882 0.120 14 23119433 5 prime UTR variant G/A snv 0.36 3
rs12803915 0.882 0.120 11 65444508 non coding transcript exon variant G/A snv 0.16 0.17 3
rs1296957097 0.882 0.120 22 28719401 missense variant A/G snv 3
rs1310678797
VDR
0.882 0.120 12 47857143 missense variant C/T snv 7.0E-06 3
rs1361742125 0.882 0.120 5 143399842 missense variant T/C snv 4.0E-06 7.0E-06 3
rs138047632 0.882 0.120 21 45525860 missense variant A/G snv 2.4E-03 2.2E-03 3
rs140422742 0.882 0.120 7 99778046 missense variant T/C;G snv 7.6E-05 6.3E-05 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
rs143125661 0.882 0.120 6 18149120 missense variant C/T snv 4.0E-06 7.0E-06 3
rs1482545954 0.882 0.120 19 54982407 missense variant C/T snv 7.0E-06 3
rs1573613 0.882 0.120 12 11894684 3 prime UTR variant T/C snv 0.48 3
rs200378616 0.882 0.120 7 87544938 missense variant G/C;T snv 4.0E-05; 8.0E-06 3
rs2742038 0.882 0.120 10 101137330 3 prime UTR variant C/T snv 0.16 3
rs35134728 0.882 0.120 1 11787277 3 prime UTR variant -/AGA delins 3
rs368005287 0.882 0.120 7 99762071 stop gained C/T snv 1.2E-05 7.0E-06 3
rs3731246 0.882 0.120 9 21971990 intron variant C/G snv 0.11 3
rs3737966 0.882 0.120 1 11787702 3 prime UTR variant C/T snv 0.55 3
rs3758149
GGH
0.882 0.120 8 63039169 upstream gene variant G/A snv 0.24 3
rs3794012 0.882 0.120 11 8248697 intron variant T/C snv 0.32 3
rs41320251 0.882 0.120 20 3213196 missense variant C/A;G snv 3