ClinVar Miner

Submissions for variant NM_005559.4(LAMA1):c.8736A>G (p.Ser2912=)

gnomAD frequency: 0.02505  dbSNP: rs78279255
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 RCV000962574 SCV001109664 benign not provided 2025-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000962574 SCV005248260 benign not provided criteria provided, single submitter not provided

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