ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.341-81del

gnomAD frequency: 0.00860  dbSNP: rs570638580
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001592434 SCV001824057 likely benign not provided 2021-01-12 criteria provided, single submitter clinical testing

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