ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.918A>G (p.Glu306=)

gnomAD frequency: 0.00002  dbSNP: rs760806762
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000554754 SCV000623356 likely benign Bloom syndrome 2024-10-29 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256335 SCV002533177 uncertain significance Hereditary cancer-predisposing syndrome 2021-04-23 criteria provided, single submitter curation
Ambry Genetics RCV002256335 SCV002683279 likely benign Hereditary cancer-predisposing syndrome 2020-09-21 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Natera, Inc. RCV000554754 SCV001460764 likely benign Bloom syndrome 2020-09-16 no assertion criteria provided clinical testing

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