Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58 3
rs11157596
LOC105370401
1.000 0.040 14 22438076 intron variant G/A snv 0.58 1
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs9653226
MYCNOS ; MYCN
0.882 0.080 2 15939632 intron variant C/T snv 0.54 3
rs1860517 1.000 0.040 7 38291209 downstream gene variant A/G snv 0.53 1
rs221634
LIN28B
0.851 0.080 6 105080213 3 prime UTR variant T/A snv 0.52 4
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs760019
LOC105370401
1.000 0.040 14 22414183 intron variant G/A snv 0.51 1
rs2736964 1.000 0.040 7 38305168 upstream gene variant T/C snv 0.51 1
rs6441201
RSRC1
0.882 0.080 3 158460535 intron variant G/A snv 0.51 3
rs2367486 1.000 0.040 7 142784320 upstream gene variant A/G snv 0.50 2
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs996165
LOC112267867
1.000 0.040 14 22485696 upstream gene variant C/T snv 0.50 1
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs2053710
BARD1
1.000 0.040 2 214751984 intron variant C/T snv 0.49 1
rs12587
KRAS
0.827 0.200 12 25205894 3 prime UTR variant T/G snv 0.49 5
rs204938
LMO1
0.882 0.080 11 8256650 intron variant C/T snv 0.49 3
rs2027801 1.000 0.040 7 142712861 upstream gene variant G/A snv 0.48 1
rs7147975 1.000 0.040 14 22022482 intergenic variant A/G snv 0.48 1
rs6572351 1.000 0.040 14 22268415 intron variant C/T snv 0.47 1
rs979027 1.000 0.040 14 22020269 intergenic variant G/A snv 0.46 1
rs11103603 0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46 4
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10