Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 8
rs10519717
LOC105377462
0.851 0.080 4 144559188 intron variant T/C snv 0.21 4
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 4
rs1053566
MAP2K7
0.882 0.080 19 7911079 missense variant C/T snv 3
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1057519719
BRAF
1.000 0.080 7 140781593 missense variant T/C snv 2
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 4
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 4
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519984
TP53
0.882 0.080 17 7673777 missense variant G/C;T snv 3
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1057520015
ROCK1
1.000 0.080 18 20955181 missense variant G/A snv 2
rs1057520037
EGFR
1.000 0.080 7 55174782 missense variant G/C snv 1