ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.8644G>A (p.Val2882Met)

gnomAD frequency: 0.00016  dbSNP: rs138024644
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001949202 SCV002210814 benign LAMA2-related muscular dystrophy 2024-09-05 criteria provided, single submitter clinical testing

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