Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805008 0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 16
rs1800407 0.807 0.200 15 27985172 missense variant C/T snv 4.7E-02 4.9E-02 10
rs1800414 0.851 0.200 15 27951891 missense variant T/A;C snv 4.0E-06; 4.5E-02 4
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs3213119 1.000 0.040 5 159316780 missense variant C/A snv 2.1E-02 2.1E-02 1
rs5352 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 5
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs11568953
EGF
1.000 0.040 4 109963240 synonymous variant A/G snv 9.7E-03 1.0E-02 1
rs1805009 0.790 0.280 16 89920138 missense variant G/A;C snv 4.0E-06; 9.1E-03 9
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs3136025 0.882 0.080 17 35002030 missense variant G/A snv 6.8E-03 2.7E-02 3
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs28720291 1.000 0.040 11 61322299 synonymous variant C/T snv 5.9E-03 6.3E-03 1
rs1110400 1.000 0.040 16 89919722 missense variant T/C snv 5.6E-03 6.6E-03 3
rs11547464 1.000 0.040 16 89919683 missense variant G/A snv 5.3E-03 4.7E-03 2
rs1805006 0.790 0.080 16 89919510 missense variant C/A;G snv 5.2E-03; 4.0E-06 8
rs151322829 0.882 0.080 15 30905792 missense variant C/G;T snv 4.2E-03 5
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs34090186 0.882 0.080 16 89919458 missense variant G/A snv 9.6E-04 2.7E-04 3
rs201326893 1.000 0.040 16 89919714 stop gained C/A snv 8.4E-04 5.4E-04 1