ClinVar Miner

Submissions for variant NM_001963.6(EGF):c.941-9C>A

gnomAD frequency: 0.00088  dbSNP: rs147880662
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 RCV000880105 SCV001023176 benign not provided 2024-04-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002478997 SCV002801716 likely benign Renal hypomagnesemia 4 2021-11-04 criteria provided, single submitter clinical testing

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