Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10849433
LOC105369624
0.776 0.080 12 6297738 regulatory region variant T/C snv 0.38 10
rs10849438 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 9
rs10904849
CUBN
0.790 0.080 10 16955267 intron variant G/A;T snv 0.25 9
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11064437
SPSB2
0.790 0.080 12 6872998 splice acceptor variant C/T snv 9.3E-02 9
rs11085466
LOC101929007
0.790 0.080 19 21569009 intron variant G/C snv 0.23 10
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
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
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 10
rs11169572 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 9
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 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
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs113569514
SLCO2A1
0.790 0.080 3 134029945 intron variant T/C snv 0.23 9
rs114436839
PLCH1
0.790 0.080 3 155691561 intron variant G/A snv 1.8E-03 9
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17