ClinVar Miner

Submissions for variant NM_001079866.2(BCS1L):c.432A>C (p.Arg144=)

dbSNP: rs1335460302
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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 RCV002200985 SCV002481403 likely benign not provided 2023-07-06 criteria provided, single submitter clinical testing

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