ClinVar Miner

Submissions for variant NM_003001.5(SDHC):c.*20T>G

gnomAD frequency: 0.00002  dbSNP: rs587778662
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410848 SCV000487767 uncertain significance Paragangliomas 3 2015-12-01 criteria provided, single submitter clinical testing
ITMI RCV000122005 SCV000086216 not provided not specified 2013-09-19 no assertion provided reference population

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