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: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 1.000 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: C0023343
Disease: Leprosy
Leprosy
0.010 1.000 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: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
0.010 < 0.001 1 2015 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.010 1.000 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: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 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: C0031090
Disease: Periodontal Diseases
Periodontal Diseases
0.010 1.000 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: C0029443
Disease: Osteomyelitis
Osteomyelitis
0.010 1.000 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C3826128
Disease: Infection in children
Infection in children
0.010 1.000 1 2019 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0042384
Disease: Vasculitis
Vasculitis
0.010 1.000 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: C0043144
Disease: Wheezing
Wheezing
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.010 1.000 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: C0003615
Disease: Appendicitis
Appendicitis
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy
0.010 1.000 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: C4303092
Disease: Cystic echinococcosis
Cystic echinococcosis
0.010 1.000 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: C0947751
Disease: Vascular inflammations
Vascular inflammations
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
0.010 1.000 1 2009 2009
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome
0.010 1.000 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: C0040425
Disease: Tonsillitis
Tonsillitis
0.010 1.000 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: C0023241
Disease: Legionnaires' Disease
Legionnaires' Disease
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Secondary malignant neoplasm of lymph node
0.010 1.000 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: C4023560
Disease: Generalized periodontitis
Generalized periodontitis
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0038522
Disease: Subacute Sclerosing Panencephalitis
Subacute Sclerosing Panencephalitis
0.010 1.000 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: C0085605
Disease: Liver Failure
Liver Failure
0.010 1.000 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: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 1.000 1 2012 2012