Variant: rs1554629007 

    present in Gene: SMARCA2
    present in Chromosome: 9
    Position on Chromosome: 2115958
    Alleles of this Variant: T/G

rs1554629007 in SMARCA2 gene and Dysmorphic features PMID 25169058 2014 Phenotype and genotype in Nicolaides-Baraitser syndrome.

PMID 8287185 1993 An unusual syndrome with mental retardation and sparse hair.

PMID 25249037 2015 Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.

PMID 22366787 2012 Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.

PMID 19606471 2009 Nicolaides-Baraitser syndrome: Delineation of the phenotype.

PMID 14564210 2003 Nicolaides-Baraitser syndrome: confirmatory report of a syndrome with sparse hair, mental retardation, and short stature and metacarpals.

rs1554629007 in SMARCA2 gene and Movement Disorders PMID 25169058 2014 Phenotype and genotype in Nicolaides-Baraitser syndrome.

PMID 25249037 2015 Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.

PMID 19606471 2009 Nicolaides-Baraitser syndrome: Delineation of the phenotype.

PMID 8287185 1993 An unusual syndrome with mental retardation and sparse hair.

PMID 14564210 2003 Nicolaides-Baraitser syndrome: confirmatory report of a syndrome with sparse hair, mental retardation, and short stature and metacarpals.

PMID 22366787 2012 Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.