Disease: Pancreatic carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 5
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs4759313
HOTAIR
0.851 0.120 12 53965290 intron variant T/A snv 0.51 4
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1810205
CUBN
0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs2585428
CYP24A1
0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs2607775
XPC ; LSM3
0.807 0.160 3 14178595 5 prime UTR variant C/G snv 0.42 0.43 8
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs4619
IGFBP1
0.882 0.160 7 45893070 missense variant A/G snv 0.36 0.38 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs4269383
LOC105378072 ; LOC101928923
0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 3
rs5768709
TAFA5
0.925 0.120 22 48533757 intron variant A/G snv 0.36 2