ClinVar Miner

Submissions for variant NM_005689.4(ABCB6):c.1452+4A>G

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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 RCV003429550 SCV004151431 likely benign not provided 2022-06-01 criteria provided, single submitter clinical testing ABCB6: BP4

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