ClinVar Miner

Submissions for variant NM_001041.4(SI):c.2737-12_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 RCV002127262 SCV002407219 benign not provided 2023-12-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494293 SCV002804320 likely benign Sucrase-isomaltase deficiency 2021-07-26 criteria provided, single submitter clinical testing

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