ClinVar Miner

Submissions for variant NM_144498.4(OSBPL2):c.1340+34GCGGGGAGGCCCCACACACACCTGGGGACG[4]

dbSNP: rs3831241
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656408 SCV001862612 benign not provided 2019-08-13 criteria provided, single submitter clinical testing

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