TRNF, tRNA, 4558

N. diseases: 148; N. variants: 6
Disease: MELAS Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906734
rs387906734
Entrez Id: 4558
Gene Symbol: TRNF
TRNF
CUI: C0162671
Disease:
MELAS Syndrome 		A 0.700 CausalMutation CLINVAR Limited clinical relevance of mitochondrial DNA mutation and gene expression analyses in ovarian cancer. 18842121 2008
dbSNP: rs387906734
rs387906734
Entrez Id: 4558
Gene Symbol: TRNF
TRNF
CUI: C0162671
Disease:
MELAS Syndrome 		A 0.700 CausalMutation CLINVAR Mitochondrial DNA mutations in human colonic crypt stem cells. 14597761 2003