ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.3558-302G>A

gnomAD frequency: 0.02216  dbSNP: rs117675557
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
GeneDx RCV001591970 SCV001826276 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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