ClinVar Miner

Submissions for variant NM_020975.6(RET):c.73+9278G>A

gnomAD frequency: 0.00019  dbSNP: rs537638504
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409618 SCV000489847 likely benign Multiple endocrine neoplasia type 2B 2016-05-19 criteria provided, single submitter clinical testing
Counsyl RCV000410768 SCV000489848 likely benign Multiple endocrine neoplasia type 2A 2016-05-19 criteria provided, single submitter clinical testing

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