ClinVar Miner

Submissions for variant NM_000305.3(PON2):c.708T>G (p.Val236=)

gnomAD frequency: 0.00009  dbSNP: rs758886833
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000923954 SCV001069453 likely benign not provided 2018-08-16 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003479248 SCV004222901 benign not specified 2023-11-20 criteria provided, single submitter clinical testing

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