ClinVar Miner

Submissions for variant NM_001041.4(SI):c.2737-23dup

dbSNP: rs11452619
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000373121 SCV000441983 likely benign Sucrase-isomaltase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000373121 SCV002802285 likely benign Sucrase-isomaltase deficiency 2021-11-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005090550 SCV005791016 benign not provided 2024-12-18 criteria provided, single submitter clinical testing

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