ClinVar Miner

Submissions for variant NM_003470.3(USP7):c.1097A>C (p.Asp366Ala)

dbSNP: rs2549235509
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001270376 SCV001450656 uncertain significance Hao-Fountain syndrome 2020-06-16 no assertion criteria provided clinical testing

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