ClinVar Miner

Submissions for variant NM_201384.3(PLEC):c.5556G>A (p.Ala1852=)

gnomAD frequency: 0.00001  dbSNP: rs782115169
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000366793 SCV000344832 uncertain significance not provided 2016-09-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002059285 SCV002431359 likely benign Epidermolysis bullosa simplex 5B, with muscular dystrophy; Epidermolysis bullosa simplex, Ogna type; Epidermolysis bullosa simplex 5C, with pyloric atresia; Autosomal recessive limb-girdle muscular dystrophy type 2Q; Epidermolysis bullosa simplex with nail dystrophy 2020-11-24 criteria provided, single submitter clinical testing

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