rs2241883, FABP1

N. diseases: 14
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.
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.700 1.000 1 2018 2018
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.030 1.000 3 2016 2018
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.020 1.000 2 2008 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1 2007 2007
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1 2007 2007
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1.000 1 2016 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1 2018 2018
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1.000 1 2008 2008
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1 2018 2018
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1 2018 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1.000 1 2007 2007
Pain
CUI: C0030193
Disease: Pain
196 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1.000 1 2016 2016
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 0.010 1.000 1 2016 2016