ClinVar Miner

Submissions for variant NM_001375567.1(FOCAD):c.5005-23C>T

gnomAD frequency: 0.18053  dbSNP: rs13301875
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 RCV001667459 SCV001889099 benign not provided 2019-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001667459 SCV005269894 benign not provided criteria provided, single submitter not provided

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