rs6656401, CR1

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.776 0.200 1 207518704 intron variant A/G;T snv 0.900 1.000 17 2009 2019
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.776 0.200 1 207518704 intron variant A/G;T snv 0.070 1.000 7 2011 2018
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.776 0.200 1 207518704 intron variant A/G;T snv 0.010 1.000 1 2012 2012
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.776 0.200 1 207518704 intron variant A/G;T snv 0.010 1.000 1 2012 2012
Cerebral Amyloid Angiopathy
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
22 0.776 0.200 1 207518704 intron variant A/G;T snv 0.010 1.000 1 2012 2012
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.776 0.200 1 207518704 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.776 0.200 1 207518704 intron variant A/G;T snv 0.010 1 2011 2011
Recurrent depression
CUI: C0221480
Disease: Recurrent depression
12 0.776 0.200 1 207518704 intron variant A/G;T snv 0.010 1.000 1 2012 2012