ClinVar Miner

Submissions for variant NM_003001.5(SDHC):c.-32T>C

gnomAD frequency: 0.01342  dbSNP: rs115782155
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000293942 SCV000482986 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000444699 SCV000518996 benign not specified 2016-06-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001810872 SCV001157663 benign not provided 2019-07-22 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000444699 SCV002552537 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316509 SCV004015424 benign Paragangliomas 3 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001810872 SCV005285766 benign not provided criteria provided, single submitter not provided

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