rs11724635, BST1

N. diseases: 3
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 4 15735478 intron variant C/A;G snv 0.43 0.880 0.846 13 2011 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.925 0.080 4 15735478 intron variant C/A;G snv 0.43 0.010 1.000 1 2017 2017
Caffeine related disorders
CUI: C0236734
Disease: Caffeine related disorders
56 0.925 0.080 4 15735478 intron variant C/A;G snv 0.43 0.010 1.000 1 2012 2012