ClinVar Miner

Submissions for variant NM_002979.5(SCP2):c.831C>T (p.Gly277=)

dbSNP: rs2150173502
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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 RCV002185368 SCV002355193 likely benign not provided 2022-07-11 criteria provided, single submitter clinical testing

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