ClinVar Miner

Submissions for variant NM_001379180.1(ESRRB):c.1261C>A (p.Arg421=)

dbSNP: rs948871827
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002158629 SCV002465264 likely benign not provided 2022-07-06 criteria provided, single submitter clinical testing

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