ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.1668+117A>G

gnomAD frequency: 0.00662  dbSNP: rs146957221
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
GeneDx RCV001546558 SCV001766095 likely benign not provided 2018-08-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001546558 SCV005225143 likely benign not provided criteria provided, single submitter not provided

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