ClinVar Miner

Submissions for variant NM_033026.6(PCLO):c.10668T>A (p.Pro3556=)

gnomAD frequency: 0.00066  dbSNP: rs144871999
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001727406 SCV001962057 likely benign not provided 2021-07-01 criteria provided, single submitter clinical testing
Invitae RCV001727406 SCV002401551 benign not provided 2023-12-08 criteria provided, single submitter clinical testing

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