rs5174, LRP8

N. diseases: 10
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.
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.700 1.000 1 2014 2014
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
CUI: C1832662
Disease: MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
3 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.700 0
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.060 0.833 6 2007 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.050 1.000 5 2007 2014
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.030 1.000 3 2009 2014
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2009 2009
Borderline Personality Disorder
CUI: C0006012
Disease: Borderline Personality Disorder
82 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2016 2016
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2016 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.010 1 2012 2012
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 0.010 1.000 1 2016 2016