Source: ALL

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: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.040 0.750 4 2012 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0017152
Disease: Gastritis
Gastritis
0.040 1.000 4 2007 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection
0.040 1.000 4 2018 2020
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.040 0.750 4 2004 2012
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.040 0.750 4 2016 2020
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.500 4 2011 2018
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
Infection caused by Helicobacter pylori
0.040 1.000 4 2012 2019
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.040 0.500 4 2006 2018
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection
0.040 0.750 4 2013 2020
dbSNP: rs11536889
rs11536889
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 1.000 3 2011 2014
dbSNP: rs11536889
rs11536889
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.030 1.000 3 2011 2014
dbSNP: rs11536889
rs11536889
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 1.000 3 2016 2019
dbSNP: rs1927911
rs1927911
0.658 0.640 9 117707776 intron variant A/G snv 0.62
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2013 2015
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2013 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.030 1.000 3 2006 2009
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections
0.030 1.000 3 2006 2010
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.030 1.000 3 2008 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.030 0.667 3 2010 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.030 0.667 3 2007 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.030 1.000 3 2009 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0025303
Disease: Meningococcal Infections
Meningococcal Infections
0.030 1.000 3 2001 2009
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0024530
Disease: Malaria
Malaria
0.030 1.000 3 2007 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.030 1.000 3 2008 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0338437
Disease: Neurocysticercosis
Neurocysticercosis
0.030 1.000 3 2010 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.030 1.000 3 2004 2018