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: rs111278892
rs111278892 		1.000 0.080 19 1039324 upstream gene variant C/G;T snv 0.12
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs3795065
rs3795065 		1.000 0.080 19 1039445 upstream gene variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs3752228
rs3752228 		1.000 0.040 19 1041165 intron variant C/T snv 6.6E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs72973581
rs72973581 		1.000 0.080 19 1043104 missense variant G/A snv 4.2E-02 4.0E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs3752231
rs3752231 		1.000 0.080 19 1043639 intron variant C/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs3752232
rs3752232 		1.000 0.080 19 1043749 missense variant A/G snv 5.5E-02 0.10
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs148078867
rs148078867 		0.925 0.080 19 1044727 missense variant C/G snv 2.2E-04 2.1E-04
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs148078867
rs148078867 		0.925 0.080 19 1044727 missense variant C/G snv 2.2E-04 2.1E-04
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.900 1.000 11 2011 2019
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.030 1.000 3 2015 2020
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0497327
Disease: Dementia
Dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0162534
Disease: Prion Diseases
Prion Diseases 		Infections; Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3764650
rs3764650 		0.790 0.200 19 1046521 intron variant T/G snv 0.14
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs4147915
rs4147915 		19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4147915
rs4147915 		19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4147915
rs4147915 		19 1049306 synonymous variant C/A;G snv 0.18; 4.0E-06
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs115550680
rs115550680 		1.000 0.080 19 1050421 intron variant A/G snv 1.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.830 0.667 3 2013 2019
dbSNP: rs12151021
rs12151021 		19 1050875 intron variant A/G;T snv 0.69
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs12151021
rs12151021 		19 1050875 intron variant A/G;T snv 0.69
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs12151021
rs12151021 		19 1050875 intron variant A/G;T snv 0.69
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2018 2018
dbSNP: rs143718918
rs143718918 		19 1051007 missense variant G/A;T snv 1.1E-03
CUI: C4282179
Disease: ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO
ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO 		0.700 1.000 3 2015 2018