ClinVar Miner

Submissions for variant NM_001128431.4(SLC39A14):c.313G>T (p.Glu105Ter)

dbSNP: rs879253764
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000234923 SCV000292246 pathogenic Hypermanganesemia with dystonia 2 2022-01-19 no assertion criteria provided literature only
GeneReviews RCV000234923 SCV000612139 not provided Hypermanganesemia with dystonia 2 no assertion provided literature only

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