Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Acute appendicitis NOS (disorder)
CUI: C0085693
Disease: Acute appendicitis NOS (disorder)
2 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Chorioamnionitis
CUI: C0008495
Disease: Chorioamnionitis
2 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2019 2019
Stomach Diseases
CUI: C0038354
Disease: Stomach Diseases
3 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2019 2019
Cerebral Thrombosis
CUI: C0079102
Disease: Cerebral Thrombosis
7 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Spastic Quadriplegia
CUI: C0426970
Disease: Spastic Quadriplegia
7 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2013 2013
Tooth Loss
CUI: C0080233
Disease: Tooth Loss
8 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Cerebral arterial thrombosis
CUI: C0795687
Disease: Cerebral arterial thrombosis
9 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Appendicitis
CUI: C0003615
Disease: Appendicitis
10 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Leukomalacia, Periventricular
CUI: C0023529
Disease: Leukomalacia, Periventricular
10 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2014 2014
Cachexia
CUI: C0006625
Disease: Cachexia
11 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2014 2014
Thrombosis of cerebral veins
CUI: C0151945
Disease: Thrombosis of cerebral veins
11 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Congenital Dysplasia Of The Hip
CUI: C4551649
Disease: Congenital Dysplasia Of The Hip
27 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.020 1.000 2 2015 2017
Drug-Induced Liver Disease
CUI: C0860207
Disease: Drug-Induced Liver Disease
29 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2018 2018
Lumbar disc disease
CUI: C0221775
Disease: Lumbar disc disease
30 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2017 2017
Membranous glomerulonephritis
CUI: C0017665
Disease: Membranous glomerulonephritis
33 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2010 2010
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2017 2017
Intervertebral Disc Degeneration
CUI: C0158266
Disease: Intervertebral Disc Degeneration
47 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2011 2011
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1 2013 2013
Cone-Rod Dystrophy 2
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
51 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2015 2015
Respiratory Distress Syndrome, Adult
60 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2019 2019
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2014 2014
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
80 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2014 2014
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2019 2019
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2011 2011
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.020 1.000 2 2009 2019