Disease: Pancreatic carcinoma
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
rs1034925236
NR5A2
0.925 0.120 1 200048258 missense variant G/C snv 2
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1049074086
CTSD
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs11571836
BRCA2
0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs11644322
WWOX
0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs11655237
LINC00511 ; LINC00673
0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs1176026649
CBR4 ; PALLD
0.851 0.120 4 168921582 missense variant C/T snv 7.2E-06 4
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3