Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906666
CBL
0.827 0.080 11 119278182 missense variant A/C;G snv 5
rs74315450 0.851 0.120 21 34859485 missense variant C/T snv 5
rs780634396 0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs869312953 0.851 0.120 1 64846735 missense variant G/T snv 5
rs10251201 0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs1188975135 0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs121913452 0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs1360698171 0.851 0.080 1 182584103 missense variant T/C snv 4
rs753000469 0.851 0.200 1 212859113 missense variant C/T snv 4.0E-06 4
rs754944509 0.851 0.080 17 42690793 missense variant C/T snv 4.4E-05 4
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs2308950 0.882 0.040 1 15507011 missense variant C/G;T snv 4.0E-06; 1.1E-02 3
rs766274360 0.882 0.040 16 2713697 missense variant G/T snv 1.2E-05 3
rs9318227 0.882 0.080 13 73926833 intron variant T/A;C snv 3
rs10931910 0.925 0.040 2 200659013 intron variant A/G;T snv 2
rs1258094111 0.925 0.040 14 24575388 missense variant C/T snv 4.0E-06 2
rs201820837 0.925 0.040 12 11869532 missense variant G/A;T snv 2.4E-05; 6.4E-05 2
rs754894156 0.925 0.040 21 34834544 missense variant C/T snv 4.0E-06 2
rs765669662 0.925 0.040 8 85465317 missense variant G/A;T snv 2.0E-05; 4.0E-06 2
rs227092 1.000 0.040 11 108366056 3 prime UTR variant G/A;C;T snv 1
rs1408538785 0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs762613037 0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs1482518887 0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73