ClinVar Miner

Submissions for variant NM_020975.6(RET):c.73+9494A>C

gnomAD frequency: 0.78499  dbSNP: rs2506004
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515286 SCV001723324 benign Multiple endocrine neoplasia, type 2 2021-12-18 criteria provided, single submitter clinical testing
GeneDx RCV000860559 SCV001884628 benign not provided 2019-06-14 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 20977903)

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