ClinVar Miner

Submissions for variant NM_001145358.2(SIN3A):c.1343A>G (p.Lys448Arg)

dbSNP: rs1595904471
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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 RCV000883995 SCV001027344 likely benign not provided 2017-08-10 criteria provided, single submitter clinical testing

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