ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.2226C>T (p.Asn742=)

gnomAD frequency: 0.00004  dbSNP: rs530906240
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000770213 SCV000901643 likely benign Cardiomyopathy 2016-11-22 criteria provided, single submitter clinical testing
Invitae RCV001516419 SCV001724693 benign Dilated cardiomyopathy 1JJ 2023-09-26 criteria provided, single submitter clinical testing
GeneDx RCV000869114 SCV001830458 likely benign not provided 2021-01-18 criteria provided, single submitter clinical testing

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