ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.322C>T (p.Arg108Trp)

gnomAD frequency: 0.00001  dbSNP: rs1298033161
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
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 RCV000824935 SCV000965970 likely benign Noonan syndrome no assertion criteria provided clinical testing

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