ClinVar Miner

Submissions for variant NM_000398.7(CYB5R3):c.733+259T>C

gnomAD frequency: 0.06322  dbSNP: rs2071843
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001635706 SCV001847798 benign not provided 2021-06-18 criteria provided, single submitter clinical testing

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