ClinVar Miner

Submissions for variant NM_018713.3(SLC30A10):c.314_322del (p.Ala105_Pro107del)

dbSNP: rs281860285
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023870 SCV000045161 pathogenic Hypermanganesemia with dystonia, polycythemia, and cirrhosis 2012-03-09 no assertion criteria provided literature only
GeneReviews RCV000023870 SCV000054647 not provided Hypermanganesemia with dystonia, polycythemia, and cirrhosis no assertion provided literature only

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