ClinVar Miner

Submissions for variant NM_020975.6(RET):c.337+29G>A

gnomAD frequency: 0.00005  dbSNP: rs578158807
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411638 SCV000489863 likely benign Multiple endocrine neoplasia type 2B 2016-06-03 criteria provided, single submitter clinical testing
Counsyl RCV000409650 SCV000489864 likely benign Multiple endocrine neoplasia type 2A 2016-06-03 criteria provided, single submitter clinical testing

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