ClinVar Miner

Submissions for variant NM_001041.4(SI):c.636-22_636-19del

dbSNP: rs558953371
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 RCV002136940 SCV002401914 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486905 SCV002799073 benign Sucrase-isomaltase deficiency 2021-07-16 criteria provided, single submitter clinical testing

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