ClinVar Miner

Submissions for variant NM_138281.3(DLX4):c.204C>T (p.Ser68=)

gnomAD frequency: 0.00041  dbSNP: rs200579401
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
Invitae RCV000902008 SCV001046407 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002505308 SCV002809302 likely benign Orofacial cleft 15 2022-04-06 criteria provided, single submitter clinical testing

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