Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs387906555
rs387906555
DCC ; LINC01917
1.000 0.080 18 53526629 missense variant C/A;G;T snv 4.0E-06; 8.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 0
dbSNP: rs2229080
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2004 2004
dbSNP: rs9944880
rs9944880
DCC
0.882 0.120 18 53125996 intron variant G/A snv 5.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2018 2018