ClinVar Miner

Submissions for variant NM_003001.4(SDHC):c.*1181_*1182insA

gnomAD frequency: 0.11567  dbSNP: rs34067216
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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 RCV000329756 SCV000350291 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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