ClinVar Miner

Submissions for variant NM_000274.4(OAT):c.966A>T (p.Thr322=)

dbSNP: rs1951417723
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 RCV001280140 SCV001671598 likely benign Ornithine aminotransferase deficiency 2022-02-03 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280140 SCV001467294 uncertain significance Ornithine aminotransferase deficiency 2020-04-11 no assertion criteria provided clinical testing

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