Variant: rs869025340 

    present in Gene: BRAF
    present in Chromosome: 7
    Position on Chromosome: 140777032
    Alleles of this Variant: A/C;G;T

rs869025340 in BRAF gene and Dysmorphic features PMID 18039235 2007 Neurological complications of cardio-facio-cutaneous syndrome.

PMID 16825433 2006 The cardiofaciocutaneous syndrome.

PMID 19206169 2009 Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.

PMID 16523510 2006 LEOPARD syndrome: clinical diagnosis in the first year of life.

PMID 4386970 1968 Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.

PMID 5771505 1969 Multiple lentigenes syndrome.

PMID 18413255 2008 Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome.

PMID 23875798 2013 The RASopathies.

rs869025340 in BRAF gene and Movement Disorders PMID 19206169 2009 Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.

PMID 18413255 2008 Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome.

PMID 5771505 1969 Multiple lentigenes syndrome.

PMID 4386970 1968 Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.

PMID 23875798 2013 The RASopathies.

PMID 16523510 2006 LEOPARD syndrome: clinical diagnosis in the first year of life.

PMID 18039235 2007 Neurological complications of cardio-facio-cutaneous syndrome.

PMID 16825433 2006 The cardiofaciocutaneous syndrome.

rs869025340 in BRAF gene and Multiple congenital anomalies PMID 18039235 2007 Neurological complications of cardio-facio-cutaneous syndrome.

PMID 16825433 2006 The cardiofaciocutaneous syndrome.

PMID 18413255 2008 Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome.

PMID 4386970 1968 Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.

PMID 23875798 2013 The RASopathies.

PMID 19206169 2009 Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.

PMID 16523510 2006 LEOPARD syndrome: clinical diagnosis in the first year of life.

PMID 5771505 1969 Multiple lentigenes syndrome.

rs869025340 in BRAF gene and Muscle hypotonia PMID 4386970 1968 Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.

PMID 5771505 1969 Multiple lentigenes syndrome.

PMID 18039235 2007 Neurological complications of cardio-facio-cutaneous syndrome.

PMID 16825433 2006 The cardiofaciocutaneous syndrome.

PMID 23875798 2013 The RASopathies.

PMID 19206169 2009 Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.

PMID 18413255 2008 Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome.

PMID 16523510 2006 LEOPARD syndrome: clinical diagnosis in the first year of life.