Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607911 0.851 0.200 2 47403192 start lost A/C;G;T snv 5.1E-05; 1.4E-05 8
rs188957694 0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs372043866 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs587779333 0.851 0.200 7 6009019 start lost T/A;C;G snv 4.0E-06; 2.8E-05 10
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs767606327 4 99613118 missense variant T/C;G snv 1.2E-05; 4.0E-06 2
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs577715207 0.827 0.160 3 189886413 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 8
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs786202567 1.000 0.120 7 5992027 missense variant T/A;C snv 4.0E-06 1.4E-05 5
rs1245554802 0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs1418016570 6 161973326 missense variant G/C snv 4.0E-06 1
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214