ClinVar Miner

Submissions for variant NM_001281740.3(FHOD3):c.958-89A>G

gnomAD frequency: 0.80476  dbSNP: rs2644253
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 RCV001676312 SCV001895295 benign not provided 2018-09-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676312 SCV005247834 benign not provided criteria provided, single submitter not provided

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