ClinVar Miner

Submissions for variant NM_005559.4(LAMA1):c.7051-9T>A

gnomAD frequency: 0.00001  dbSNP: rs1472738373
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 RCV000936309 SCV001082074 likely benign not provided 2023-06-09 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002282407 SCV002572358 likely benign not specified 2024-12-11 criteria provided, single submitter clinical testing

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