Disease: Malignant neoplasm of large intestine
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 9
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs12682374
POU5F1B ; PCAT1 ; CCAT2 ; CASC8
0.790 0.080 8 127398703 intron variant C/A;G;T snv 9
rs1330889
LINC00446 ; OBI1-AS1
0.790 0.080 13 78035480 intron variant T/A;C snv 9
rs1445011 0.790 0.080 5 40280100 intergenic variant T/C;G snv 9
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs16959063
FMN1 ; LOC107984089
0.790 0.080 15 32813529 intron variant G/A;C snv 9
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 13
rs189583 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 10
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv 9