rs11136000, CLU

N. diseases: 17
Source: BEFREE ×
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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
968 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.900 0.913 21 2009 2018
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.100 1.000 12 2010 2018
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
94 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.040 1.000 4 2013 2019
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
223 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.020 1.000 2 2013 2018
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
27 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2016 2016
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2019 2019
Dementia
CUI: C0497327
Disease: Dementia
165 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2014 2014
Diabetes
CUI: C0011847
Disease: Diabetes
611 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
714 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2019 2019
Forgetful
CUI: C0542476
Disease: Forgetful
18 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2016 2016
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
206 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2017 2017
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
80 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2017 2017
Memory impairment
CUI: C0233794
Disease: Memory impairment
33 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2016 2016
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
90 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2013 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2011 2011
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2014 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1332 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2010 2010