ClinVar Miner

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

dbSNP: rs11452619
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002097113 SCV002326689 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498092 SCV002813029 likely benign Sucrase-isomaltase deficiency 2022-03-24 criteria provided, single submitter clinical testing

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