rs1057519086, NDUFAF6

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 17
CUI: C4748786
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17
6 1.000 8 95052177 missense variant A/G snv 0.800 0