ClinVar Miner

Submissions for variant NM_025136.4(OPA3):c.277G>A (p.Gly93Ser)

dbSNP: rs80356524
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 RCV000004462 SCV000024635 pathogenic Optic atrophy 3 2004-09-01 no assertion criteria provided literature only
GeneReviews RCV000004462 SCV000041512 not provided Optic atrophy 3 no assertion provided literature only

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