ClinVar Miner

Submissions for variant NM_024596.5(MCPH1):c.2214+32439C>A

dbSNP: rs6559167
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
Breakthrough Genomics, Breakthrough Genomics RCV004712135 SCV005272197 benign not provided criteria provided, single submitter not provided
Genetic Services Laboratory, University of Chicago RCV000146294 SCV000193560 likely benign not specified no assertion criteria provided clinical testing

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