ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.1088T>A (p.Ile363Asn)

dbSNP: rs2145972483
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV002274490 SCV002559234 not provided Dystonia 12 no assertion provided literature only

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