ClinVar Miner

Submissions for variant NM_003001.4(SDHC):c.*1012G>T

dbSNP: rs886045484
Minimum review status: Collection method:
Minimum conflict level:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000328424 SCV000350288 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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