ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1198-19G>C

dbSNP: rs757759855
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Mendelian Genomics, University Medical Centre Ljubljana RCV000626906 SCV000747609 uncertain significance Hemimegalencephaly 2017-01-01 criteria provided, single submitter clinical testing

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