Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs4796030
LIG3
0.827 0.120 17 35003131 3 prime UTR variant A/C snv 0.66 6
rs74315352
PARK7
0.807 0.080 1 7984930 missense variant A/C snv 1.4E-04 5.9E-04 6
rs1362575880
PSEN1
0.851 0.120 14 73192840 missense variant A/C snv 4.0E-06 4
rs17065417
LIN28B
0.882 0.080 6 104958399 intron variant A/C snv 0.10 3
rs11587304 1.000 0.040 1 143653074 upstream gene variant A/C snv 0.83 1
rs1964986
PRSS1
1.000 0.040 7 142739784 upstream gene variant A/C snv 0.59 1
rs2213212 1.000 0.040 7 142698925 downstream gene variant A/C snv 0.63 1
rs2293732
LOC105370401 ; LOC112267867
1.000 0.040 14 22473159 intron variant A/C snv 0.44 1
rs2736969 1.000 0.040 7 38304355 upstream gene variant A/C snv 0.11 1
rs2736973 1.000 0.040 7 38302014 upstream gene variant A/C snv 0.86 1
rs6953248 1.000 0.040 7 38316814 downstream gene variant A/C snv 0.14 1
rs6966279 1.000 0.040 7 38329947 upstream gene variant A/C snv 0.14 1
rs8020193
LOC112267867 ; LOC105370401
1.000 0.040 14 22470475 intron variant A/C snv 0.43 1
rs34787247
LIN28A
0.851 0.200 1 26428582 3 prime UTR variant A/C;G snv 4
rs13034994
MYCNOS
0.882 0.080 2 15938513 non coding transcript exon variant A/C;G snv 3
rs227867
LOC105370401 ; LOC112267867
1.000 0.040 14 22484872 upstream gene variant A/C;G snv 1
rs2734224 1.000 0.040 7 142780878 upstream gene variant A/C;G snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs587781960
CHEK2
0.882 0.080 22 28689164 missense variant A/C;G;T snv 1.3E-05; 7.3E-05 4
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38