Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs11247957
LIN28A
0.882 0.080 1 26429683 3 prime UTR variant G/A snv 0.21 3
rs1301478248
CASP9
0.882 0.080 1 15495395 missense variant C/T snv 3
rs138085133
LOC101928216 ; EXTL1
0.882 0.080 1 26022729 missense variant C/G;T snv 8.4E-04; 4.0E-06 3
rs11579261 1.000 0.040 1 143544453 intron variant T/A;C snv 1
rs11587304 1.000 0.040 1 143653074 upstream gene variant A/C snv 0.83 1
rs137974312
CAMTA1
1.000 0.040 1 7738307 missense variant C/T snv 2.1E-03 1.3E-03 1
rs17161949 1.000 0.040 1 143550435 intron variant T/C snv 6.4E-02 1
rs17162074
LOC112268273
1.000 0.040 1 143569860 intron variant G/A snv 6.5E-02 1
rs17162082 1.000 0.040 1 143545399 intron variant C/T snv 5.0E-02 1
rs3853524 1.000 0.040 1 143665797 intergenic variant C/A;T snv 1
rs41278952
CAMTA1
1.000 0.040 1 7737443 missense variant C/G snv 0.12 9.8E-02 1
rs6673776 1.000 0.040 1 143566021 intron variant T/A;C snv 3.3E-02 1
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs121908513
SPAST
0.807 0.280 2 32116145 missense variant T/A snv 6
rs1048108
SNHG31 ; BARD1
0.827 0.120 2 214809500 missense variant G/A snv 0.38 0.33 5
rs57961569
MYCNOS ; MYCN
0.827 0.200 2 15939643 intron variant G/A;C snv 5
rs6435862
BARD1
0.827 0.160 2 214807822 intron variant G/A;C;T snv 5
rs863225285
ALK
0.851 0.080 2 29209789 missense variant T/G snv 5
rs3768716
BARD1
0.851 0.080 2 214771070 intron variant T/C snv 0.16 4
rs535080528
NFU1
0.851 0.120 2 69431903 splice region variant T/A;C snv 4.0E-06 4