ClinVar Miner

Submissions for variant NM_001041.4(SI):c.374-11dup

dbSNP: rs11313475
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 RCV002197868 SCV002351967 benign not provided 2023-04-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498201 SCV002813027 likely benign Sucrase-isomaltase deficiency 2022-03-22 criteria provided, single submitter clinical testing

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