ClinVar Miner

Submissions for variant NM_001999.4(FBN2):c.1849+5G>A

dbSNP: rs1561426412
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000680531 SCV000807936 likely benign Connective tissue disorder 2018-06-01 criteria provided, single submitter clinical testing

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