ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.703C>A (p.Arg235Ser)

dbSNP: rs201227908
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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 RCV000714585 SCV000845293 uncertain significance Congenital muscular dystrophy due to LMNA mutation 2018-08-07 criteria provided, single submitter clinical testing

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