ClinVar Miner

Submissions for variant NM_006796.3(AFG3L2):c.1479G>A (p.Pro493=)

gnomAD frequency: 0.00006  dbSNP: rs761143170
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 RCV000903457 SCV001047924 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000903457 SCV001145388 benign not provided 2018-09-14 criteria provided, single submitter clinical testing

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