ClinVar Miner

Submissions for variant NM_006662.3(SRCAP):c.6576G>A (p.Glu2192=)

dbSNP: rs886044120
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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) RCV000311802 SCV000343534 uncertain significance not provided 2016-08-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000311802 SCV004619913 likely benign not provided 2023-06-29 criteria provided, single submitter clinical testing

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