ClinVar Miner

Submissions for variant NM_001001344.3(ATP2B3):c.1686C>G (p.Arg562=)

dbSNP: rs140240114
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000896940 SCV001041054 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000896940 SCV001501571 likely benign not provided 2020-10-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000896940 SCV005206860 likely benign not provided criteria provided, single submitter not provided

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