Source: GWASCAT

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: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 8 2008 2019
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 8 2008 2019
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 8 2008 2019
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 8 2008 2019
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 8 2008 2019
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 8 2008 2019
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 8 2008 2019
dbSNP: rs3817334
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 8 2010 2018
dbSNP: rs4939827
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 8 2007 2019
dbSNP: rs4939827
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 8 2007 2019
dbSNP: rs4939827
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 8 2007 2019
dbSNP: rs4939827
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 8 2007 2019
dbSNP: rs4939827
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 8 2007 2019
dbSNP: rs4939827
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 8 2007 2019
dbSNP: rs55661361
rs55661361
NRGN
1.000 0.040 11 124744061 intron variant G/A snv 0.43
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 8 2014 2019
dbSNP: rs633185
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 8 2011 2018
dbSNP: rs880315
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 8 2011 2018
dbSNP: rs10132280
rs10132280 		14 25458973 intergenic variant C/A snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2019
dbSNP: rs116843064
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 7 2014 2019
dbSNP: rs116843064
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 7 2014 2019
dbSNP: rs11740474
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 7 2014 2019
dbSNP: rs12446632
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2019
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 7 2011 2019
dbSNP: rs1327235
rs1327235 		20 10988382 intron variant A/G snv 0.46
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 7 2011 2018
dbSNP: rs1516725
rs1516725
DGKG ; ETV5
0.925 0.120 3 186106215 intron variant T/C snv 0.86
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2013 2019