ClinVar Miner

Submissions for variant NM_032802.4(SPPL2A):c.1035C>A (p.Gly345=)

dbSNP: rs76947817
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002220101 SCV002363969 likely benign not provided 2021-06-13 criteria provided, single submitter clinical testing

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