Source: ALL

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: rs7259620
rs7259620
0.925 0.120 19 44904531 upstream gene variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 2 2013 2019
dbSNP: rs7259620
rs7259620
0.925 0.120 19 44904531 upstream gene variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 1.000 2 2018 2019
dbSNP: rs449647
rs449647
0.925 0.120 19 44905307 upstream gene variant A/T snv 0.21
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.730 1.000 4 2009 2018
dbSNP: rs449647
rs449647
0.925 0.120 19 44905307 upstream gene variant A/T snv 0.21
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
0.010 1.000 1 2011 2011
dbSNP: rs769446
rs769446
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.740 1.000 5 2009 2018
dbSNP: rs769446
rs769446
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs769446
rs769446
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs769446
rs769446
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs769446
rs769446
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
0.010 1.000 1 2011 2011
dbSNP: rs769446
rs769446
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 0.950 20 2009 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 3 2012 2013
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
Low density lipoprotein cholesterol measurement
0.700 1.000 3 2012 2013
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.020 1.000 2 2016 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.020 1.000 2 2009 2009
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.010 1.000 1 2017 2017
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
0.010 1.000 1 2019 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2009 2009
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0.010 1.000 1 2015 2015
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
0.010 1.000 1 2019 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0236848
Disease: Age-related cognitive decline
Age-related cognitive decline
0.010 1.000 1 2017 2017
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.010 < 0.001 1 2019 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012