Disease: Pancreatic carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1322648460
LOC100507144 ; CD44
0.776 0.320 11 35139332 frameshift variant G/- delins 9
rs1336539869
CDK4
0.925 0.120 12 57751681 missense variant C/G snv 2
rs1339638227
CDKN2A
0.925 0.120 9 21971119 missense variant T/C snv 4.3E-06 2
rs1370041903
PRKN
0.925 0.120 6 161350185 stop gained G/A snv 3
rs141095230
MGMT
0.925 0.120 10 129536277 missense variant C/A;T snv 8.0E-06; 5.2E-05 2
rs1448106115
PMS2
0.925 0.120 7 5989944 missense variant T/C snv 4.0E-06 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs150495372
ADH1B
0.925 0.120 4 99313834 missense variant C/T snv 3.7E-04 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1555525012
TP53
0.882 0.200 17 7673603 missense variant G/A snv 3
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs1799966
BRCA1
0.807 0.280 17 43071077 missense variant T/A;C snv 5.2E-05; 0.35 8
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs1801270
CDKN1A
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 13
rs199769221
PRSS1
0.790 0.280 7 142751920 missense variant G/A;C;T snv 8.0E-05; 4.0E-06 8