Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.900 0.913 21 2009 2018
dbSNP: rs9331888
rs9331888
CLU ; MIR6843
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 		0.880 1.000 8 2009 2019
dbSNP: rs2279590
rs2279590
CLU
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 		0.840 1.000 4 2009 2019
dbSNP: rs9331896
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.820 1.000 2 2013 2019
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.100 1.000 12 2010 2018
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder 		0.040 1.000 4 2013 2019
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.020 1.000 2 2013 2018
dbSNP: rs9331949
rs9331949
CLU ; EPHX2
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 		0.020 1.000 2 2013 2017
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2019 2019
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.010 1.000 1 2014 2014
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.010 1.000 1 2013 2013
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		0.010 1.000 1 2017 2017
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2010 2010
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2011 2011
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0233794
Disease: Memory impairment
Memory impairment 		0.010 1.000 1 2016 2016
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2017 2017
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2019 2019
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0542476
Disease: Forgetful
Forgetful 		0.010 1.000 1 2016 2016
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0497327
Disease: Dementia
Dementia 		0.010 1.000 1 2014 2014
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		0.010 1.000 1 2019 2019
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 1.000 1 2016 2016
dbSNP: rs141383962
rs141383962
CLU
0.882 0.040 8 27605112 missense variant C/G;T snv 7.2E-05 1.0E-04
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 1998 1998
dbSNP: rs141383962
rs141383962
CLU
0.882 0.040 8 27605112 missense variant C/G;T snv 7.2E-05 1.0E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 1998 1998
dbSNP: rs141383962
rs141383962
CLU
0.882 0.040 8 27605112 missense variant C/G;T snv 7.2E-05 1.0E-04
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 1998 1998
dbSNP: rs1532278
rs1532278
CLU
0.925 0.080 8 27608798 non coding transcript exon variant T/C snv 0.68
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.010 1.000 1 2014 2014