Gene: SCO2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs946234163
rs946234163
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. 10852545

2000
dbSNP: rs892141220
rs892141220
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. 14720311

2004
dbSNP: rs866001342
rs866001342
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome. 15781193

2005
dbSNP: rs797044455
rs797044455
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029

1999
dbSNP: rs797044455
rs797044455
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. 10852545

2000
dbSNP: rs786205098
rs786205098
TYMP ; SCO2
A 0.700 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029

1999
dbSNP: rs786205097
rs786205097
TYMP ; SCO2
AG 0.700 CausalMutation CLINVAR

dbSNP: rs773785934
rs773785934
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029

1999
dbSNP: rs770277446
rs770277446
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients. 12529715

2003
dbSNP: rs764275775
rs764275775
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. 21933806

2011
dbSNP: rs761665644
rs761665644
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR

dbSNP: rs201685922
rs201685922
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. 10852545

2000
dbSNP: rs1556488264
rs1556488264
TYMP ; SCO2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1556486467
rs1556486467
TYMP ; SCO2
GA 0.700 CausalMutation CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. 14720311

2004
dbSNP: rs1556486107
rs1556486107
TYMP ; SCO2
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1556486029
rs1556486029
TYMP ; SCO2
TG 0.700 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029

1999
dbSNP: rs149977726
rs149977726
TYMP ; SCO2
C 0.800 CausalMutation CLINVAR Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029

1999
dbSNP: rs1471478620
rs1471478620
TYMP ; SCO2
AG 0.700 GeneticVariation CLINVAR

dbSNP: rs121913042
rs121913042
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026

2005
dbSNP: rs121913041
rs121913041
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1). 19748572

2009
dbSNP: rs121913041
rs121913041
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026

2005
dbSNP: rs121913040
rs121913040
TYMP ; SCO2
G 0.700 CausalMutation CLINVAR Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026

2005
dbSNP: rs121913040
rs121913040
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. 21933806

2011
dbSNP: rs121913040
rs121913040
TYMP ; SCO2
A 0.700 CausalMutation CLINVAR Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. 21933806

2011
dbSNP: rs121913039
rs121913039
TYMP ; SCO2
T 0.700 CausalMutation CLINVAR Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026

2005