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: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis
0.030 1.000 3 2004 2010
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.030 0.667 3 2009 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011847
Disease: Diabetes
Diabetes
0.030 1.000 3 2004 2018
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: 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: C3873491
Disease: Invasive meningococcal disease
Invasive meningococcal disease
0.020 1.000 2 2009 2009
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1864267
Disease: Endotoxin Hyporesponsiveness
Endotoxin Hyporesponsiveness
0.020 1.000 2 2005 2008
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.020 1.000 2 2004 2010
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
Leishmaniasis, Cutaneous
0.020 1.000 2 2011 2013
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.020 0.500 2 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2012 2013
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.020 1.000 2 2006 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Respiratory Syncytial Virus Infections
0.020 1.000 2 2006 2007
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.020 1.000 2 2003 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0155877
Disease: Allergic asthma
Allergic asthma
0.020 1.000 2 2004 2020
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2012 2013
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2
0.020 1.000 2 2009 2011
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.020 1.000 2 2017 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Malignant neoplasm of gastrointestinal tract
0.020 1.000 2 2013 2013
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
0.020 1.000 2 2010 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.020 1.000 2 2009 2011
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome
0.020 0.500 2 2010 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis
0.020 1.000 2 2012 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.020 0.500 2 2011 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.020 0.500 2 2005 2015