ClinVar Miner

Submissions for variant NM_000132.4(F8):c.2113+471_2113+473dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003436899 SCV004166014 benign not provided 2022-12-01 criteria provided, single submitter clinical testing F8: BS1, BS2

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