ClinVar Miner

Submissions for variant NM_001041.4(SI):c.3423+10A>G

dbSNP: rs200899300
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 RCV002101296 SCV002395640 likely benign not provided 2023-02-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507980 SCV002805794 likely benign Sucrase-isomaltase deficiency 2021-12-03 criteria provided, single submitter clinical testing

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