ClinVar Miner

Submissions for variant NM_001281740.3(FHOD3):c.2022-133T>C

gnomAD frequency: 0.69499  dbSNP: rs479570
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 RCV001724984 SCV001950716 benign not provided 2018-09-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001724984 SCV005247845 benign not provided criteria provided, single submitter not provided

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