VCV000445854.7 Observations – ClinVar – NCBI

1 SCV000610624.1 Center for Pediatric Genomic Medicine,Children’s Mercy Hospital and Clinics Benign criteria provided,
single submitter clinical testing not provided (not provided ) germline 1 SCV000700353.2 Eurofins NTD, LLC Uncertain significance criteria provided,
single submitter clinical testing 1 not provided (unknown ) germline 1 Single Heterozygote www.egl-eurofins.com/emvclass/emvclass.php?approved_symbol=CYP21A2 mixed 1 SCV001137083.1 Mendelics Benign criteria provided,
single submitter clinical testing Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (unknown ) unknown 1 SCV000841734.3 Athena Diagnostics Inc Uncertain significance criteria provided,
single submitter clinical testing not provided (unknown ) unknown PubMed: 25630015
PubMed: 15110320
PubMed: 16788163
PubMed: 23241443
PubMed: 32289882
PubMed: 19204079
PubMed: 22841790
PubMed: 21228398
PubMed: 17119906
PubMed: 23359706
PubMed: 21534945
PubMed: 19505723
PubMed: 21169732 1 SCV001469962.1 Quest Diagnostics Nichols Institute San Juan Capistrano Uncertain significance criteria provided,
single submitter clinical testing not provided (unknown ) unknown PubMed: 25630015
PubMed: 15110320
PubMed: 16788163
PubMed: 23241443
PubMed: 32289882
PubMed: 19204079
PubMed: 22841790
PubMed: 21228398
PubMed: 17119906
PubMed: 23359706
PubMed: 21534945
PubMed: 19505723
PubMed: 21169732 1 SCV001914277.1 GeneDx Benign criteria provided,
single submitter clinical testing Not Provided (yes ) germline This variant is associated with the following publications: (PMID: 21228398, 23359706, 15110320)