ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.891T>C (p.Asp297=)

dbSNP: rs2151149684
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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 RCV001454467 SCV001658194 likely benign Bloom syndrome 2020-02-29 criteria provided, single submitter clinical testing

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