ClinVar Miner

Submissions for variant NM_000236.3(LIPC):c.968C>T (p.Thr323Met)

gnomAD frequency: 0.00007  dbSNP: rs573111255
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
Clinical Genetics, Academic Medical Center RCV001700664 SCV001920960 uncertain significance not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001700664 SCV001963551 uncertain significance not provided no assertion criteria provided clinical testing

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