ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.6370-191_6370-187del

gnomAD frequency: 0.03337  dbSNP: rs377727314
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001568620 SCV001792526 likely benign not provided 2019-11-26 criteria provided, single submitter clinical testing

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