ClinVar Miner

Submissions for variant NM_000236.3(LIPC):c.1169+31T>C

gnomAD frequency: 0.25934  dbSNP: rs77010273
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 RCV001641443 SCV001859764 benign not provided 2018-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001641443 SCV005289486 benign not provided criteria provided, single submitter not provided

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