ClinVar Miner

Submissions for variant NM_020774.4(MIB1):c.-17C>T

gnomAD frequency: 0.00074  dbSNP: rs561980800
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 RCV001699666 SCV001922818 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001726637 SCV001963585 likely benign not provided no assertion criteria provided clinical testing

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