ClinVar Miner

Submissions for variant NM_001041.4(SI):c.2737-17_2737-11del

dbSNP: rs11452619
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002087051 SCV002327740 likely benign not provided 2022-07-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002493996 SCV002798596 likely benign Sucrase-isomaltase deficiency 2021-11-16 criteria provided, single submitter clinical testing

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