ClinVar Miner

Submissions for variant NM_001375567.1(FOCAD):c.907-49A>G

gnomAD frequency: 0.83736  dbSNP: rs7875153
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 RCV001691645 SCV001913466 benign not provided 2019-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001691645 SCV005269854 benign not provided criteria provided, single submitter not provided

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