ClinVar Miner

Submissions for variant NM_000382.3(ALDH3A2):c.798+5G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000169484 SCV000220936 likely pathogenic Sjögren-Larsson syndrome 2014-12-09 criteria provided, single submitter literature only
Génétique des Maladies du Développement, Hospices Civils de Lyon RCV000169484 SCV001738833 pathogenic Sjögren-Larsson syndrome no assertion criteria provided clinical testing

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