rs267606896, CYTB;ND5

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.
Leigh Disease
CUI: C0023264
Disease: Leigh Disease
114 0.882 0.200 MT 13084 missense variant A/T snv 0.700 1.000 3 2002 2007
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
8 0.882 0.200 MT 13084 missense variant A/T snv 0.700 0
MELAS Syndrome
CUI: C0162671
Disease: MELAS Syndrome
53 0.882 0.200 MT 13084 missense variant A/T snv 0.700 0