ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.325-18543_325-18542insAGAG

dbSNP: rs34201045
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
Mendelics RCV000987372 SCV001136655 likely benign Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001712837 SCV001944549 benign not provided 2018-07-07 criteria provided, single submitter clinical testing

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