ClinVar Miner

Submissions for variant NM_017755.5(NSUN2):c.-217delT

dbSNP: rs8192124
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
Illumina Laboratory Services, Illumina RCV000270497 SCV000458108 likely benign Intellectual Disability, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001643073 SCV001856993 benign not provided 2018-10-01 criteria provided, single submitter clinical testing

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