ClinVar Miner

Submissions for variant NM_001042750.2(STAG2):c.1535-3del

dbSNP: rs36097834
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001391293 SCV001593264 likely benign Holoprosencephaly 13, X-linked 2021-05-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070255 SCV002378274 benign not provided 2024-08-27 criteria provided, single submitter clinical testing

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