ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.2556-12G>C

dbSNP: rs2151177995
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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 RCV002088784 SCV002388147 likely benign Bloom syndrome 2021-09-20 criteria provided, single submitter clinical testing

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