ClinVar Miner

Submissions for variant NM_018206.6(VPS35):c.171G>A (p.Met57Ile)

gnomAD frequency: 0.00001  dbSNP: rs183554824
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002225672 SCV002504258 likely benign not provided 2020-03-11 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
GeneReviews RCV000577231 SCV000679655 not provided Parkinson disease 17 no assertion provided literature only

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