APOE, apolipoprotein E, 348

N. diseases: 1049; N. variants: 62
Disease: Presenile dementia ×
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: rs429358
rs429358 		0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.030 1.000 3 2001 2018
dbSNP: rs1233347077
rs1233347077 		0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2006 2006
dbSNP: rs405509
rs405509 		0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 < 0.001 1 2019 2019
dbSNP: rs440446
rs440446 		0.807 0.200 19 44905910 missense variant C/G;T snv 0.60
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 < 0.001 1 2019 2019
dbSNP: rs7412
rs7412 		0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 < 0.001 1 2010 2010
dbSNP: rs748703149
rs748703149 		0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 < 0.001 1 2020 2020