ClinVar Miner

Submissions for variant NM_004055.5(CAPN5):c.297+11G>A

gnomAD frequency: 0.00012  dbSNP: rs374146255
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 RCV002154566 SCV002469426 likely benign not provided 2024-10-15 criteria provided, single submitter clinical testing
AiLife Diagnostics, AiLife Diagnostics RCV002154566 SCV002503333 uncertain significance not provided 2020-05-13 criteria provided, single submitter clinical testing

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