ClinVar Miner

Submissions for variant NM_001281740.3(FHOD3):c.2321A>G (p.Gln774Arg)

gnomAD frequency: 0.02276  dbSNP: rs61735994
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 RCV001768180 SCV002008624 likely benign not provided 2024-06-26 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Breakthrough Genomics, Breakthrough Genomics RCV001768180 SCV005215308 likely benign not provided criteria provided, single submitter not provided

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