Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 21
rs113994087
ALK
1.000 0.071 2 29209798 missense variant C/A,T snp 4
rs137852567
AR
0.846 0.179 X 67717595 missense variant A/G snp 1
rs28904921 0.756 0.286 11 108329202 missense variant T/G snp 4.0E-05 6.4E-05 7
rs587776547 0.923 0.250 11 108331885 inframe deletion CTCTAGAATT/C in-del 2.8E-05 4
rs121913348 0.801 0.214 7 140781617 missense variant C/A,G,T snp 5
rs80357906 0.846 0.179 17 43057065 frameshift variant G/GG in-del 1.8E-04 1.6E-04 7
rs28897672 0.756 0.214 17 43106487 missense variant A/C,G,T snp 3.2E-05 6
rs80357783 0.923 0.179 17 43124030 frameshift variant C/CG,CCT,CT in-del 4.0E-06 6
rs1800747 0.923 0.179 17 43063952 splice acceptor variant C/A,G,T snp 5
rs28897696 0.801 0.179 17 43063903 missense variant G/A,C,T snp 2.8E-05; 4.0E-06; 2.0E-05 3.2E-05 5
rs41293465 0.923 0.179 17 43045767 stop gained G/A snp 1.2E-05 5
rs62625308 0.923 0.179 17 43091924 stop gained G/A,C snp 1.2E-05 5
rs80356962 1.000 0.179 17 43047666 stop gained C/T snp 4.0E-06 4
rs80356978 1.000 0.179 17 43092809 stop gained C/A,T snp 4
rs80357006 1.000 0.179 17 43092274 stop gained A/C,G,T snp 1.2E-05 4
rs80357086 0.878 0.179 17 43106480 stop gained A/G,T snp 4
rs80357123 1.000 0.179 17 43057078 stop gained G/A,T snp 1.2E-05 3.2E-05 4
rs80357287 1.000 0.179 17 43124096 start lost T/C snp 4
rs80357303 1.000 0.179 17 43071113 stop gained T/A,G snp 4.0E-06 4
rs80357310 1.000 0.179 17 43091870 stop gained C/A,G snp 4.0E-06 4
rs80357522 1.000 0.179 17 43093570 frameshift variant CT/C in-del 4
rs80357580 1.000 0.179 17 43067652 frameshift variant AGTTA/A in-del 4
rs80357701 1.000 0.179 17 43092199 frameshift variant TTGCT/T in-del 4
rs80357706 1.000 0.179 17 43093125 frameshift variant TCA/T in-del 4.0E-06 4