Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9951307 0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs8192597 1.000 0.040 18 907674 synonymous variant G/A snv 0.73 0.67 1
rs80356779 0.776 0.320 11 68780662 missense variant G/A snv 3.2E-05 5.6E-05 10
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs786205867 0.882 0.080 1 111787039 missense variant C/T snv 3
rs77931234 0.925 0.120 1 75761161 missense variant A/C;G snv 3.3E-03 3
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs7626962 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs758995 1.000 0.040 7 31064948 intron variant G/A snv 0.12 0.17 1
rs757532106 0.763 0.120 3 38550500 stop gained G/A snv 4.5E-05 4.9E-05 9
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs72878794 1.000 0.040 18 26866839 intron variant C/A;T snv 8.1E-02 1
rs72552293 0.925 0.120 3 32140231 missense variant A/G snv 2.5E-03 2.9E-03 2
rs72546668 0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 8
rs72466451 0.925 0.160 2 197498763 missense variant T/C snv 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs45546039 0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs3906956 1.000 0.040 18 26856350 missense variant A/G snv 1
rs368660364 1.000 0.040 20 33408748 missense variant C/T snv 1.6E-05 2.8E-05 1
rs2856966 0.925 0.080 18 907709 missense variant A/G snv 0.19 0.18 2
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72