Source: BEFREE

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: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 < 0.001 1 2016 2016
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 < 0.001 1 2016 2016
dbSNP: rs11536878
rs11536878
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs11536878
rs11536878
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic
0.010 < 0.001 1 2014 2014
dbSNP: rs11536878
rs11536878
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 < 0.001 1 2014 2014
dbSNP: rs11536878
rs11536878
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 < 0.001 1 2015 2015
dbSNP: rs11536889
rs11536889
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.010 < 0.001 1 2017 2017
dbSNP: rs11536889
rs11536889
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 < 0.001 1 2019 2019
dbSNP: rs1927911
rs1927911
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 < 0.001 1 2019 2019
dbSNP: rs1927911
rs1927911
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 < 0.001 1 2017 2017
dbSNP: rs1927911
rs1927911
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 < 0.001 1 2017 2017
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia
0.010 < 0.001 1 2007 2007
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 < 0.001 1 2016 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.010 < 0.001 1 2013 2013
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.010 < 0.001 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
0.010 < 0.001 1 2018 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 < 0.001 1 2016 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0085423
Disease: Gram-Negative Bacterial Infections
Gram-Negative Bacterial Infections
0.010 < 0.001 1 2011 2011
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0002871
Disease: Anemia
Anemia
0.010 < 0.001 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0022568
Disease: Keratitis
Keratitis
0.010 < 0.001 1 2012 2012
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0.010 < 0.001 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis
0.010 < 0.001 1 2003 2003
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0155733
Disease: Atherosclerosis of aorta
Atherosclerosis of aorta
0.010 < 0.001 1 2007 2007
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2004 2004