ClinVar Miner

Submissions for variant NM_000398.7(CYB5R3):c.45A>G (p.Pro15=)

gnomAD frequency: 0.00329  dbSNP: rs111649710
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000897687 SCV001041844 benign not provided 2025-01-20 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000897687 SCV004563853 benign not provided 2024-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000897687 SCV005274164 benign not provided criteria provided, single submitter not provided

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