ClinVar Miner

Submissions for variant NM_000289.6(PFKM):c.-9+86A>G

gnomAD frequency: 0.03415  dbSNP: rs58373242
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
GeneDx RCV001787535 SCV002030953 benign not provided 2021-12-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001787535 SCV005232941 benign not provided criteria provided, single submitter not provided

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