Disease: Adenocarcinoma of lung (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 8
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2290035
ARNTL
0.827 0.160 11 13386224 intron variant T/A snv 0.46 5
rs2352028
GPC5
0.851 0.080 13 91792975 intron variant C/G;T snv 6
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 10
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47 8
rs3816360
ARNTL
0.807 0.120 11 13346203 intron variant T/C snv 0.58 6
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs425366
CHL1
0.851 0.080 3 283727 intron variant A/C snv 0.56 4
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 5
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs4953354
EPAS1
0.827 0.120 2 46348249 intron variant A/G snv 0.22 5