ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.1901-319A>G

gnomAD frequency: 0.30725  dbSNP: rs11145357
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 RCV001647868 SCV001857279 benign not provided 2018-07-05 criteria provided, single submitter clinical testing

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