rs121918454
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations.
|
26607044 |
2016 |
rs397507510
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.
|
27069254 |
2016 |
rs397507510
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genomic Classification and Prognosis in Acute Myeloid Leukemia.
|
27276561 |
2016 |
rs397507512
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Clonal and microclonal mutational heterogeneity in high hyperdiploid acute lymphoblastic leukemia.
|
27683039 |
2016 |
rs397507506
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing.
|
25914815 |
2015 |
rs397507510
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia.
|
25395418 |
2015 |
rs397507549
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Rapidly progressive hypertrophic cardiomyopathy in an infant with Noonan syndrome with multiple lentigines: palliative treatment with a rapamycin analog.
|
25708222 |
2015 |
rs121918454
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Juvenile myelomonocytic leukaemia and Noonan syndrome.
|
25097206 |
2014 |
rs121918454
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Behavioral profile in RASopathies.
|
24458522 |
2014 |
rs397507510
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Juvenile myelomonocytic leukaemia and Noonan syndrome.
|
25097206 |
2014 |
rs397507510
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Juvenile myelomonocytic leukaemia and Noonan syndrome.
|
25097206 |
2014 |
rs397507510
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition.
|
25253770 |
2014 |
rs397507512
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
The spectrum of somatic mutations in high-risk acute myeloid leukaemia with -7/del(7q).
|
24931631 |
2014 |
rs397507512
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Juvenile myelomonocytic leukaemia and Noonan syndrome.
|
25097206 |
2014 |
rs397507518
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Diagnosis of Noonan syndrome and related disorders using target next generation sequencing.
|
24451042 |
2014 |
rs397507518
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Molecular characterization of Chilean patients with a clinical diagnosis of Noonan syndrome.
|
24150203 |
2014 |
rs397516810
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Juvenile myelomonocytic leukaemia and Noonan syndrome.
|
25097206 |
2014 |
rs397516810
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Pectus excavatum and carinatum.
|
24821303 |
2014 |
rs121918468
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Atrioventricular canal defect in patients with RASopathies.
|
22781091 |
2013 |
rs121918468
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.
|
23321623 |
2013 |
rs397507506
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.
|
23321623 |
2013 |
rs397507510
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome.
|
23756559 |
2013 |
rs397507549
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Atrioventricular canal defect in patients with RASopathies.
|
22781091 |
2013 |
rs727503380
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clinical and biological implications of driver mutations in myelodysplastic syndromes.
|
24030381 |
2013 |
rs121918470
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Autoimmune disease and multiple autoantibodies in 42 patients with RASopathies.
|
22488759 |
2012 |