ClinVar Miner

Submissions for variant NM_001145809.2(MYH14):c.973+233C>T

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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 RCV003223001 SCV003918160 benign not provided 2023-01-01 criteria provided, single submitter clinical testing MYH14: BS1, BS2

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