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: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2009 2009
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.010 1.000 1 2010 2010
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration
0.010 1.000 1 2011 2011
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 1.000 1 2011 2011
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 1.000 1 2013 2013
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.010 < 0.001 1 2013 2013
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia
0.010 1.000 1 2013 2013
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0006625
Disease: Cachexia
Cachexia
0.010 1.000 1 2014 2014
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2014 2014
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
0.010 1.000 1 2014 2014
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0023529
Disease: Leukomalacia, Periventricular
Leukomalacia, Periventricular
0.010 1.000 1 2014 2014
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 1.000 2 2008 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0003615
Disease: Appendicitis
Appendicitis
0.010 1.000 1 2015 2015