ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.3627-38A>T

gnomAD frequency: 0.04750  dbSNP: rs17104663
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 RCV001723057 SCV001947149 benign not provided 2018-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001723057 SCV005289250 benign not provided criteria provided, single submitter not provided

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