Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1562430
PCAT1 ; CASC8 ; CASC21 ; POU5F1B
0.807 0.160 8 127375606 intron variant T/C snv 0.41 6
rs16847024
GC
0.882 0.120 4 71784962 intron variant C/T snv 3.2E-02 4
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18