ClinVar Miner

Submissions for variant NM_012233.3(RAB3GAP1):c.2801del (p.Pro934fs)

dbSNP: rs730882182
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000007472 SCV000027672 pathogenic Warburg micro syndrome 1 2005-03-01 no assertion criteria provided literature only
GeneReviews RCV000007472 SCV000778357 not provided Warburg micro syndrome 1 no assertion provided literature only

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