ClinVar Miner

Submissions for variant NM_016335.6(PRODH):c.1623C>G (p.Ala541=)

dbSNP: rs16983347
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000538353 SCV000631848 benign Proline dehydrogenase deficiency 2024-01-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506308 SCV002807359 benign Proline dehydrogenase deficiency; Schizophrenia 4 2021-07-26 criteria provided, single submitter clinical testing

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