rs104893646
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
A |
0.800 |
CausalMutation |
CLINVAR |
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
|
18470948 |
2008 |
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
A |
0.800 |
CausalMutation |
CLINVAR |
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
|
18470948 |
2008 |
rs104893646
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
|
0.800 |
GeneticVariation |
UNIPROT |
Expanding the clinical spectrum of MYCN-related Feingold syndrome.
|
16906565 |
2006 |
rs104893647
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
|
0.800 |
GeneticVariation |
UNIPROT |
Expanding the clinical spectrum of MYCN-related Feingold syndrome.
|
16906565 |
2006 |
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
|
0.800 |
GeneticVariation |
UNIPROT |
Expanding the clinical spectrum of MYCN-related Feingold syndrome.
|
16906565 |
2006 |
rs104893646
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
|
0.800 |
GeneticVariation |
UNIPROT |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs104893647
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
|
0.800 |
GeneticVariation |
UNIPROT |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
|
0.800 |
GeneticVariation |
UNIPROT |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs104893647
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
T |
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
rs1057519919
|
MYCN;MYCNOS
|
Adenocarcinoma of pancreas
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs1057519919
|
MYCN;MYCNOS
|
Malignant Uterine Corpus Neoplasm
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs1057519919
|
MYCN;MYCNOS
|
NEUROBLASTOMA, SUSCEPTIBILITY TO
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs1057519919
|
MYCN;MYCNOS
|
Glioblastoma
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs1057519919
|
MYCN;MYCNOS
|
Medulloblastoma
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs754137452
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
|
18470948 |
2008 |
rs759103701
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
|
18470948 |
2008 |
rs759103701
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
Esophageal atresia with or without tracheoesophageal fistula
|
T |
0.700 |
CausalMutation |
CLINVAR |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs759103701
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
Short palpebral fissure
|
T |
0.700 |
CausalMutation |
CLINVAR |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs759103701
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
Short middle phalanx of finger
|
T |
0.700 |
CausalMutation |
CLINVAR |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs759103701
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
FEINGOLD SYNDROME 1
|
T |
0.700 |
CausalMutation |
CLINVAR |
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
|
15821734 |
2005 |
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
Esophageal Atresia
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
Microcephaly (physical finding)
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs104893648
|
Entrez Id: |
4613 |
Gene Symbol: |
MYCN |
MYCN
|
Esophageal atresia with or without tracheoesophageal fistula
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs113994115
|
MYCN;MYCNOS
|
FEINGOLD SYNDROME 1
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|