rs1568344751, UQCRFS1

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.
Acidosis, Lactic
CUI: C0001125
Disease: Acidosis, Lactic
21 1.000 0.080 19 29208159 splice acceptor variant C/G snv 0.700 0
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 1.000 0.080 19 29208159 splice acceptor variant C/G snv 0.700 0
Propionic acidemia
CUI: C0268579
Disease: Propionic acidemia
124 1.000 0.080 19 29208159 splice acceptor variant C/G snv 0.700 0