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: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.900 1.000 17 2009 2019
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.070 1.000 7 2011 2018
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		0.010 1.000 1 2012 2012
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0221480
Disease: Recurrent depression
Recurrent depression 		0.010 1.000 1 2012 2012
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.010 1.000 1 2012 2012
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 1.000 1 2012 2012
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 < 0.001 1 2011 2011
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2014 2014