Disease: Pancreatic carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1034925236
NR5A2
0.925 0.120 1 200048258 missense variant G/C snv 2
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
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs111033565
PRSS1
0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 11
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
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
rs1176026649
CBR4 ; PALLD
0.851 0.120 4 168921582 missense variant C/T snv 7.2E-06 4
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1209809979
AKR1A1
0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs12456874
LDLRAD4
0.925 0.120 18 13366863 intron variant A/G snv 0.20 2
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs1318
LOC101928045 ; PITPNC1
0.925 0.120 17 67695266 3 prime UTR variant A/G snv 0.30 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
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
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs139599857
XRCC1
0.882 0.120 19 43545922 missense variant C/G snv 1.6E-05 2.1E-05 3