ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.85G>A (p.Asp29Asn)

dbSNP: rs150662822
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001721355 SCV000530799 likely benign not provided 2019-06-26 criteria provided, single submitter clinical testing
Invitae RCV002059871 SCV002342305 likely benign Dilated cardiomyopathy 1JJ 2023-12-21 criteria provided, single submitter clinical testing
Ambry Genetics RCV002446725 SCV002676377 likely benign Cardiovascular phenotype 2018-09-10 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003330675 SCV004038030 likely benign not specified 2023-08-19 criteria provided, single submitter clinical testing

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