ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.315+255T>C

dbSNP: rs1847544780
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Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001430727 SCV001633472 likely benign not provided 2019-10-09 criteria provided, single submitter clinical testing
The ITHANET community portal, The Cyprus Institute of Neurology and Genetics RCV001078424 SCV001244638 benign beta Thalassemia 2019-11-25 no assertion criteria provided curation

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