rs7976091, VDR

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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 1.000 0.040 12 47910769 intron variant C/T snv 0.38 0.010 1.000 1 2011 2011
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 1.000 0.040 12 47910769 intron variant C/T snv 0.38 0.010 1.000 1 2014 2014