ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.6369+130T>A

gnomAD frequency: 0.96621  dbSNP: rs8012365
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722886 SCV001946957 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001722886 SCV005289227 benign not provided criteria provided, single submitter not provided

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