ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.745G>A (p.Ala249Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003234834 SCV003932798 uncertain significance Paragangliomas 5 2019-07-07 criteria provided, single submitter clinical testing

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