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: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs56404467
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs9533282
rs9533282
FRY
13 32053511 intron variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2015 2015