Disease: Malignant neoplasm of pancreas
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2585428
CYP24A1
0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs7164773
RORA
0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs879254154
PALB2
0.851 0.160 16 23621428 missense variant A/C;G snv 4