ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.699-24C>T

gnomAD frequency: 0.00272  dbSNP: rs148154982
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 RCV001558680 SCV001780679 likely benign not provided 2018-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001558680 SCV005214863 likely benign not provided criteria provided, single submitter not provided

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