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: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.030 0.667 3 2003 2014
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 1.000 2 1999 2013
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 1999 1999
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		0.010 1.000 1 2014 2014
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 1999 1999
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.010 1.000 1 2013 2013
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.010 1.000 1 2014 2014
dbSNP: rs764929617
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		0.010 1.000 1 2014 2014