ClinVar Miner

Submissions for variant NM_001281740.3(FHOD3):c.2100C>T (p.Ala700=)

dbSNP: rs146170583
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000965403 SCV001112669 benign not provided 2018-06-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000965403 SCV005247846 benign not provided criteria provided, single submitter not provided

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