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: 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: rs63749810
rs63749810
0.882 0.200 21 25891853 missense variant C/T snv
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases 0.800 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
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
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
0.700 0
dbSNP: rs63750921
rs63750921
0.882 0.200 21 25891820 missense variant G/C snv
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
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: rs1800557
rs1800557
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders
Mental Disorders 0.010 1.000 1 1994 1994
dbSNP: rs1800557
rs1800557
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 1.000 1 1994 1994
dbSNP: rs950592627
rs950592627
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 1994 1994
dbSNP: rs1800557
rs1800557
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 1.000 2 1994 1995
dbSNP: rs63750363
rs63750363
1.000 0.080 21 25897642 missense variant C/G snv 1.2E-05 7.0E-06
CUI: C0276496
Disease: Familial Alzheimer Disease (FAD)
Familial Alzheimer Disease (FAD)
Nervous System Diseases; Mental Disorders 0.010 1.000 1 1996 1996
dbSNP: rs1231783932
rs1231783932
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05
Familial Alzheimer's disease of early onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 1997 1997
dbSNP: rs1231783932
rs1231783932
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
Neoplasms 0.010 1.000 1 1997 1997
dbSNP: rs1231783932
rs1231783932
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
Neoplasms; Nervous System Diseases 0.010 1.000 1 1997 1997
dbSNP: rs1231783932
rs1231783932
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
Neoplasms 0.010 1.000 1 1997 1997
dbSNP: rs63750399
rs63750399
0.882 0.080 21 25891787 missense variant T/A;C snv
CUI: C0750901
Disease: Alzheimer Disease, Early Onset
Alzheimer Disease, Early Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 1997 1997