Variant: rs114368325 

    present in Gene: CYP24A1
    present in Chromosome: 20
    Position on Chromosome: 54158136
    Alleles of this Variant: G/A;C

rs114368325 in CYP24A1 gene and Calcium Metabolism Disorders PMID 21675912 2011 Mutations in CYP24A1 and idiopathic infantile hypercalcemia.

PMID 22047571 2011 CYP24A1 mutations in idiopathic infantile hypercalcemia.

rs114368325 in CYP24A1 gene and Hypercalcemia, Infantile, 1 PMID 25194629 2015 Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake.

PMID 26117226 2015 Calcium and bone homeostasis in heterozygous carriers of CYP24A1 mutations: A cross-sectional study.

PMID 26097993 2015 Maternal Hypercalcemia Due to Failure of 1,25-Dihydroxyvitamin-D3 Catabolism in a Patient With CYP24A1 Mutations.

PMID 23001465 2013 Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene.

PMID 23485543 2013 Intravenous pamidronate in the treatment of severe idiopathic infantile hypercalcemia.

PMID 25446019 2015 Kidney function and influence of sunlight exposure in patients with impaired 24-hydroxylation of vitamin D due to CYP24A1 mutations.

PMID 21675912 2011 Mutations in CYP24A1 and idiopathic infantile hypercalcemia.

PMID 24518185 2014 "A Case of ""Late-Onset"" Idiopathic Infantile Hypercalcemia Secondary to Mutations in the CYP24A1 Gene."

rs114368325 in CYP24A1 gene and Nephrocalcinosis PMID 21675912 2011 Mutations in CYP24A1 and idiopathic infantile hypercalcemia.

PMID 22047571 2011 CYP24A1 mutations in idiopathic infantile hypercalcemia.