ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.2163G>A (p.Ser721=)

dbSNP: rs201724038
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
Invitae RCV000939940 SCV001085796 likely benign not provided 2024-01-19 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832144 SCV002075717 likely benign Hereditary hyperinsulinism 2020-02-17 no assertion criteria provided clinical testing

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