ClinVar Miner

Submissions for variant NM_003002.4(SDHD):c.*613T>C (rs693441)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000037725 SCV000061387 benign not specified 2011-10-10 criteria provided, single submitter clinical testing This variant is classified as benign based on its high frequency in the general population (rs693441, MAF >3%).
Illumina Clinical Services Laboratory,Illumina RCV000287625 SCV000367359 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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