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: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.720 0.857 5 2009 2018
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs7679673
rs7679673 		0.677 0.440 4 105140377 intron variant C/A snv 0.50
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016