ClinVar Miner

Submissions for variant NM_000061.3(BTK):c.894+7G>A

dbSNP: rs886044875
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000290503 SCV000341782 uncertain significance not provided 2016-05-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002518002 SCV003459309 likely benign X-linked agammaglobulinemia with growth hormone deficiency 2023-12-30 criteria provided, single submitter clinical testing

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