ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.3014A>G (p.Gln1005Arg)

gnomAD frequency: 0.00006  dbSNP: rs781587803
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001844622 SCV002103780 uncertain significance not specified 2022-02-17 criteria provided, single submitter clinical testing

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