ClinVar Miner

Submissions for variant NM_000292.3(PHKA2):c.1041+22C>T

gnomAD frequency: 0.02488  dbSNP: rs41304737
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000675946 SCV001948878 benign not provided 2021-05-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000675946 SCV005274403 benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000675946 SCV000801675 benign not provided 2016-02-03 no assertion criteria provided clinical testing

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