ClinVar Miner

Submissions for variant NM_000088.4(COL1A1):c.21C>G (p.Leu7=)

dbSNP: rs760612687
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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 RCV000680482 SCV000807860 likely benign Connective tissue disorder 2018-06-01 criteria provided, single submitter clinical testing

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