ClinVar Miner

Submissions for variant NM_001370100.5(ZMYND11):c.117-4238T>A

dbSNP: rs1057517548
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410973 SCV000488202 uncertain significance Paragangliomas 5 2016-01-20 criteria provided, single submitter clinical testing

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