ClinVar Miner

Submissions for variant NM_033026.6(PCLO):c.3498G>A (p.Thr1166=)

gnomAD frequency: 0.00281  dbSNP: rs141881813
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001819366 SCV002065703 likely benign not specified 2018-09-27 criteria provided, single submitter clinical testing
Invitae RCV002074305 SCV002320962 benign not provided 2024-01-30 criteria provided, single submitter clinical testing

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