Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs17217772 0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 10
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs367597251 0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs201216664 0.851 0.080 17 51171503 missense variant A/G snv 5
rs10009228 4 40354405 missense variant A/G snv 0.78 0.76 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs438034 0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs200863613 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs767808984 0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9