ClinVar Miner

Submissions for variant NM_004357.5(CD151):c.615+44T>G

dbSNP: rs12420593
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
GeneDx RCV001570266 SCV001794531 likely benign not provided 2019-01-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001570266 SCV005223078 likely benign not provided criteria provided, single submitter not provided

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