Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 10
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs55781567
CHRNA5
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs1423493595
UBE2V1 ; TMEM189-UBE2V1
0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 5
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs760943842
ZNF436
0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs1046175
PAOX
0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv 4