rs121434428, NDUFS2

N. diseases: 1
Source: UNIPROT ×
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.
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6
CUI: C4748759
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6
3 1.000 1 161209915 missense variant C/A snv 0.800 1.000 1 2001 2001