ClinVar Miner

Submissions for variant NM_001289125.3(IFNAR2):c.55+10G>A

dbSNP: rs1469577615
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003869806 SCV004673764 likely benign not provided 2023-12-27 criteria provided, single submitter clinical testing

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