rs199951903, ND6;CYTB

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 0.120 MT 15497 missense variant G/A snv 0.020 1.000 2 2002 2002
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
49 0.925 0.120 MT 15497 missense variant G/A snv 0.010 1.000 1 2006 2006