ClinVar Miner

Submissions for variant NM_001041.4(SI):c.119-11dup

dbSNP: rs533057264
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 RCV002116172 SCV002406295 benign not provided 2023-12-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486894 SCV002801967 likely benign Sucrase-isomaltase deficiency 2021-09-01 criteria provided, single submitter clinical testing

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