rs1064792875
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121913039
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1471478620
|
|
AG |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1556486107
|
|
GC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1556488264
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs761665644
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs786205097
|
|
AG |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs149977726
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.
|
9924029 |
1999 |
rs121913036
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.
|
9924029 |
1999 |
rs1556486029
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.
|
9924029 |
1999 |
rs773785934
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.
|
9924029 |
1999 |
rs786205098
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.
|
9924029 |
1999 |
rs797044455
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.
|
9924029 |
1999 |
rs1064792865
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
|
10852545 |
2000 |
rs201685922
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
|
10852545 |
2000 |
rs797044455
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
|
10852545 |
2000 |
rs946234163
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
|
10852545 |
2000 |
rs1064792887
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
MNGIE: diarrhea and leukoencephalopathy.
|
12084896 |
2002 |
rs1064792881
|
|
AGCCGTCGTCCAGCGCCGC |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic variability in a Spanish family with MNGIE.
|
12177387 |
2002 |
rs1060499533
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.
|
12529715 |
2003 |
rs1064792879
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.
|
12529715 |
2003 |
rs770277446
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.
|
12529715 |
2003 |
rs1064792866
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
|
14720311 |
2004 |
rs1064792870
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
|
14720311 |
2004 |
rs1064792874
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
|
14720311 |
2004 |