rs7702187, SEMA5A

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 0.040 5 9332169 intron variant T/A snv 0.70 0.020 0.500 2 2008 2014
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.925 0.040 5 9332169 intron variant T/A snv 0.70 0.010 1.000 1 2006 2006