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
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
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
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
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs12456874
LDLRAD4
0.925 0.120 18 13366863 intron variant A/G snv 0.20 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 6
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs17458086
SLC2A13
0.925 0.120 12 40034837 intron variant T/C snv 1.1E-02 2
rs1810205
CUBN
0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs2073389
SMARCB1
0.925 0.120 22 23791306 intron variant C/T snv 0.59 2
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