Variant: rs1555721837 

    present in Gene: CCDC151
    present in Chromosome: 19
    Position on Chromosome: 11423933
    Alleles of this Variant: G/A

rs1555721837 in CCDC151 gene and Dysmorphic features PMID 25192045 2014 CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.

PMID 14656747 2004 Primary ciliary dyskinesia: diagnostic and phenotypic features.

PMID 24577564 2014 Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

PMID 8071978 1994 Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome).

PMID 12627427 2003 Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome.

PMID 9298603 1997 Treatment of otitis media with effusion in children with primary ciliary dyskinesia.

PMID 25224326 2014 Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia.

rs1555721837 in CCDC151 gene and Muscle hypotonia PMID 8071978 1994 Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome).

PMID 12627427 2003 Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome.

PMID 25192045 2014 CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.

PMID 14656747 2004 Primary ciliary dyskinesia: diagnostic and phenotypic features.

PMID 24577564 2014 Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

PMID 9298603 1997 Treatment of otitis media with effusion in children with primary ciliary dyskinesia.

PMID 25224326 2014 Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia.