APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
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: rs7276737
rs7276737 		21 25885689 intron variant C/T snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7279104
rs7279104 		21 25942455 non coding transcript exon variant G/A snv 2.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9636774
rs9636774 		21 25967316 intron variant C/T snv 5.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9984764
rs9984764 		21 26125180 intron variant G/A snv 1.1E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9984764
rs9984764 		21 26125180 intron variant G/A snv 1.1E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9984764
rs9984764 		21 26125180 intron variant G/A snv 1.1E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs281865161
rs281865161 		0.925 0.080 21 25897626 missense variant TC/GA mnv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63749964
rs63749964 		0.851 0.080 21 25891783 missense variant A/C snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750066
rs63750066 		0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750264
rs63750264 		0.716 0.360 21 25891784 missense variant C/A;G;T snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750399
rs63750399 		0.882 0.080 21 25891787 missense variant T/A;C snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750643
rs63750643 		0.882 0.080 21 25891793 missense variant T/C snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750671
rs63750671 		0.790 0.240 21 25891858 missense variant G/C snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750671
rs63750671 		0.790 0.240 21 25891858 missense variant G/C snv
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs63750734
rs63750734 		0.851 0.080 21 25891790 missense variant C/T snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63750921
rs63750921 		0.882 0.200 21 25891820 missense variant G/C snv
CUI: C4015785
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT 		0.700 0
dbSNP: rs63750921
rs63750921 		0.882 0.200 21 25891820 missense variant G/C snv
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs63750973
rs63750973 		0.882 0.120 21 25891792 missense variant G/A snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs63751039
rs63751039 		0.776 0.200 21 25891855 missense variant T/C snv
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs63751039
rs63751039 		0.776 0.200 21 25891855 missense variant T/C snv
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		Nervous System Diseases; Mental Disorders 0.700 0
dbSNP: rs1386984902
rs1386984902 		0.790 0.160 21 26000095 missense variant G/A snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.100 1.000 12 2003 2020
dbSNP: rs63750264
rs63750264 		0.716 0.360 21 25891784 missense variant C/A;G;T snv
CUI: C0276496
Disease: Familial Alzheimer Disease (FAD)
Familial Alzheimer Disease (FAD) 		Nervous System Diseases; Mental Disorders 0.100 0.909 11 1991 2019
dbSNP: rs63750847
rs63750847 		0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.100 0.818 11 2012 2018
dbSNP: rs572842823
rs572842823 		0.763 0.160 21 25897626 missense variant T/A;G snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.100 1.000 10 1998 2018
dbSNP: rs371425292
rs371425292 		0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.080 1.000 8 1998 2018