ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.960-7T>C

dbSNP: rs2151152020
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002152190 SCV002416303 likely benign Bloom syndrome 2021-09-25 criteria provided, single submitter clinical testing

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