ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.786C>T (p.Thr262=)

dbSNP: rs146812127
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000465711 SCV000561647 likely benign Amelocerebrohypohidrotic syndrome 2024-12-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705613 SCV005217391 likely benign not provided criteria provided, single submitter not provided

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