CLU, clusterin, 1191

N. diseases: 412; N. variants: 14
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.900 0.913 23 2009 2018
dbSNP: rs9331888
rs9331888
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.880 1.000 9 2009 2019
dbSNP: rs2279590
rs2279590
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.840 1.000 6 2009 2019
dbSNP: rs9331896
rs9331896
0.851 0.080 8 27610169 intron variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.820 1.000 6 2013 2019
dbSNP: rs1532278
rs1532278
0.925 0.080 8 27608798 non coding transcript exon variant T/C snv 0.68
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.800 1.000 1 2011 2011
dbSNP: rs4236673
rs4236673
1.000 0.080 8 27607412 intron variant A/G snv 0.70
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0162534
Disease: Prion Diseases
Prion Diseases
Infections; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs9331908
rs9331908
1.000 0.080 8 27606101 intron variant C/T snv 0.35
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.100 1.000 12 2010 2018
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.040 1.000 4 2013 2019
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.020 1.000 2 2013 2018
dbSNP: rs9331949
rs9331949
0.925 0.080 8 27597169 3 prime UTR variant T/C snv 6.2E-02 4.7E-02
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.020 1.000 2 2013 2017
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0233794
Disease: Memory impairment
Memory impairment
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0542476
Disease: Forgetful
Forgetful
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0497327
Disease: Dementia
Dementia
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.010 1.000 1 2016 2016
dbSNP: rs11136000
rs11136000
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2010 2010