ClinVar Miner

Submissions for variant NM_001375567.1(FOCAD):c.2853-41A>G

gnomAD frequency: 0.32570  dbSNP: rs7044447
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 RCV001671254 SCV001885259 benign not provided 2019-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001671254 SCV005269872 benign not provided criteria provided, single submitter not provided

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