Submissions for variant NM_003001.3(SDHC):c.*84G>C (rs201210474)

Total submissions: 8

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
CSER_CC_NCGL; University of Washington Medical Center	RCV000211525	SCV000212170	likely benign	Pheochromocytoma	2015-03-11	criteria provided, single submitter	research
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia	RCV000203076	SCV000257750	benign	Paragangliomas 3	2015-02-16	criteria provided, single submitter	clinical testing
Illumina Clinical Services Laboratory,Illumina	RCV000211525	SCV000350269	likely benign	Pheochromocytoma	2016-06-14	criteria provided, single submitter	clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen	RCV000034692	SCV000493607	likely benign	not provided	2016-07-31	criteria provided, single submitter	clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano	RCV000122004	SCV000602173	likely benign	not specified	2017-02-12	criteria provided, single submitter	clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics	RCV000122004	SCV000859979	likely benign	not specified	2018-03-07	criteria provided, single submitter	clinical testing
Biesecker Lab/Clinical Genomics Section,National Institutes of Health	RCV000034692	SCV000043488	no known pathogenicity	not provided	2012-07-13	no assertion criteria provided	research	Converted during submission to Benign.
ITMI	RCV000122004	SCV000086215	not provided	not specified	2013-09-19	no assertion provided	reference population