rs6430538, CCNT2-AS1

N. diseases: 2
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.080 2 134782397 intron variant C/T snv 0.62 0.830 1.000 6 2012 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.925 0.080 2 134782397 intron variant C/T snv 0.62 0.010 1.000 1 2017 2017