ClinVar Miner

Submissions for variant NM_033026.6(PCLO):c.9519T>C (p.Leu3173=)

dbSNP: rs117636778
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
Invitae RCV001512639 SCV001720088 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001512639 SCV002497526 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing PCLO: BP4, BP7

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