ClinVar Miner

Submissions for variant NM_004393.6(DAG1):c.804G>A (p.Gln268=)

gnomAD frequency: 0.00001  dbSNP: rs201713621
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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) RCV000336322 SCV000341222 uncertain significance not provided 2016-04-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001496228 SCV001700922 likely benign Autosomal recessive limb-girdle muscular dystrophy type 2P; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9 2018-11-16 criteria provided, single submitter clinical testing

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