Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs961150162 7 55198779 missense variant G/A;C snv 3
rs969139366 4 54277974 missense variant T/C snv 3.5E-05 3
rs1057519771 1.000 0.080 9 130872201 missense variant G/C snv 2
rs587782148 17 7676113 missense variant C/T snv 2
rs762807774 1.000 0.040 1 1228495 frameshift variant CGCGGCTCCGC/-;CGCGGCTCCGCCGCGGCTCCGC delins 7.0E-06 2
rs2073778 22 20087052 non coding transcript exon variant C/T snv 0.12 1
rs720012 22 20111059 3 prime UTR variant G/A snv 0.12 1
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1288373809 0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs773862672 0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs767808984 0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9
rs4987188 0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70