ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.577C>G (p.Pro193Ala)

dbSNP: rs1595884713
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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 RCV000824937 SCV000965972 likely benign Noonan syndrome no assertion criteria provided clinical testing

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