ClinVar Miner

Submissions for variant NM_021116.4(ADCY1):c.258C>G (p.Pro86=)

dbSNP: rs200597993
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001769909 SCV002004843 likely benign not provided 2021-10-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001769909 SCV002471248 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001769909 SCV005227321 likely benign not provided criteria provided, single submitter not provided

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