rs738409, PNPLA3

N. diseases: 88
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.
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2016 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2016 2016
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2016 2016
Liver Cirrhosis, Alcoholic
CUI: C0023891
Disease: Liver Cirrhosis, Alcoholic
15 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.790 0.800 10 2010 2017
Hepatitis, Alcoholic
CUI: C0019187
Disease: Hepatitis, Alcoholic
1 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2016 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2015 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2015 2017
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.700 1.000 1 2017 2017
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2017 2017
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.700 1.000 1 2017 2017
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.700 1.000 1 2017 2017
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.090 1.000 9 2011 2018
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.050 0.800 5 2013 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.040 1.000 4 2013 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.040 1.000 4 2013 2018
Alanine aminotransferase measurement
CUI: C0201836
Disease: Alanine aminotransferase measurement
77 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.800 1.000 3 2011 2018
Chronic liver disease
CUI: C0341439
Disease: Chronic liver disease
14 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.030 1.000 3 2015 2018
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.800 1.000 3 2011 2018
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2017 2018
Viral hepatitis
CUI: C0042721
Disease: Viral hepatitis
5 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2013 2018
22q13.3 Deletion Syndrome
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
10 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2018 2018
Asthma
CUI: C0004096
Disease: Asthma
1536 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2018 2018
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2018 2018
Chronic viral hepatitis
CUI: C0276623
Disease: Chronic viral hepatitis
8 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2018 2018
POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA
CUI: C1868117
Disease: POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA
1 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2018 2018