ClinVar Miner

Submissions for variant NM_012233.3(RAB3GAP1):c.52A>C (p.Thr18Pro)

dbSNP: rs587777154
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000087135 SCV000119996 pathogenic Warburg micro syndrome 1 2013-05-01 no assertion criteria provided literature only
GeneReviews RCV000087135 SCV000778350 not provided Warburg micro syndrome 1 no assertion provided literature only

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