Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773785934
rs773785934
Entrez Id: 1890;9997
Gene Symbol: TYMP;SCO2
TYMP;SCO2
CUI: C4551995
Disease:
Mitochondrial DNA Depletion Syndrome 1
T 0.700 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029 1999