ClinVar Miner

Submissions for variant NM_000128.4(F11):c.1576+9G>A

dbSNP: rs1561491504
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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 RCV002889628 SCV003234563 likely benign not provided 2022-08-31 criteria provided, single submitter clinical testing

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