Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs4663402
ATG16L1
0.851 0.080 2 233285017 intron variant A/T snv 5.1E-02 4
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs2237025
KIT
0.882 0.080 4 54675713 intron variant T/C snv 0.60 3
rs2238151
ALDH2
1.000 0.040 12 111774029 intron variant T/C snv 0.52 3
rs3810294
MIR3191 ; BBC3
0.882 0.120 19 47228572 intron variant C/T snv 0.14 3
rs1972597 1.000 0.040 17 77598082 intron variant T/C snv 0.31 2
rs2012775
DELEC1
1.000 0.040 9 115141569 intron variant T/C snv 0.30 2
rs3862188 1.000 0.040 1 247702471 intron variant T/C snv 0.44 2
rs4150351
BIVM-ERCC5 ; ERCC5
0.925 0.160 13 102870617 intron variant A/C;T snv 2
rs17084687
KIT
1.000 0.040 4 54716231 intron variant C/T snv 0.11 1
rs3213183
E2F1 ; NECAB3
1.000 0.040 20 33675156 intron variant G/A;C snv 1
rs3218148
LOC101928163 ; E2F2
1.000 0.040 1 23525295 intron variant G/A;C;T snv 1
rs3218203
E2F2
1.000 0.040 1 23511068 intron variant C/A;G snv 1
rs6581580
LOC105369804 ; RASSF3
1.000 0.040 12 64609189 intron variant T/C;G snv 0.45 1
rs6970262
EGFR
1.000 0.040 7 55192070 intron variant A/G snv 0.66 1
rs845561
EGFR ; EGFR-AS1
1.000 0.040 7 55185015 intron variant C/T snv 0.76 1
rs180127 0.925 0.040 17 69923642 intergenic variant G/A;C snv 2
rs229811 1.000 0.040 14 83448259 intergenic variant G/C snv 4.4E-02 1
rs11599672
LOC105378438 ; PLCE1
0.925 0.080 10 93993019 regulatory region variant T/G snv 0.21 3