Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1982151 0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 9
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2854746 0.752 0.200 7 45921046 missense variant G/A;C;T snv 0.38 14
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223