ClinVar Miner

Submissions for variant NM_004733.4(SLC33A1):c.-343G>A

gnomAD frequency: 0.60228  dbSNP: rs1131925
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 RCV001533978 SCV001750861 benign not provided 2018-07-21 criteria provided, single submitter clinical testing

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