ClinVar Miner

Submissions for variant NM_000231.3(SGCG):c.655G>A (p.Glu219Lys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003136664 SCV003819969 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2C 2020-07-21 criteria provided, single submitter clinical testing

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