ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.92+13G>T

dbSNP: rs753444453
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001438297 SCV001641169 likely benign not provided 2023-06-02 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331041 SCV004037871 uncertain significance not specified 2023-08-04 criteria provided, single submitter clinical testing
The ITHANET community portal, The Cyprus Institute of Neurology and Genetics RCV001078280 SCV001244434 benign beta Thalassemia 2019-11-25 no assertion criteria provided curation

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