ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.3768T>C (p.Asp1256=)

dbSNP: rs2151198276
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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 RCV002101563 SCV002436085 likely benign Bloom syndrome 2023-07-17 criteria provided, single submitter clinical testing

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