ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.-220CG[4]

dbSNP: rs141005341
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000405422 SCV000393399 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000313380 SCV000393400 likely benign Cardio-facio-cutaneous syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001545000 SCV001764237 likely benign not provided 2018-10-16 criteria provided, single submitter clinical testing

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