rs104894705, NDUFS7

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 3
CUI: C4748752
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3
1 0.925 0.120 19 1391006 missense variant G/A snv 5.6E-05 8.4E-05 0.800 1.000 2 1999 1999