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: rs1056836
rs1056836
0.581 0.680 2 38071060 missense variant G/C snv 0.51
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.050 1.000 5 2007 2018
dbSNP: rs10012
rs10012
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 0.500 2 2010 2014
dbSNP: rs1056827
rs1056827
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 0.500 2 2010 2018
dbSNP: rs1800440
rs1800440
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2012 2014
dbSNP: rs162558
rs162558
1.000 0.080 2 38076937 intron variant T/A;C;G snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs760025060
rs760025060
0.776 0.200 2 38074936 missense variant C/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 < 0.001 1 2012 2012