ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.872G>C (p.Gly291Ala)

dbSNP: rs1554226736
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000626260 SCV000746913 uncertain significance Merosin deficient congenital muscular dystrophy 2017-12-18 criteria provided, single submitter clinical testing

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