ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.6321+15C>T (rs2559082)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000080322 SCV000112217 benign not specified 2013-09-19 criteria provided, single submitter clinical testing
GeneDx RCV000080322 SCV000519375 benign not specified 2016-01-05 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Clinical Services Laboratory,Illumina RCV000360522 SCV000431858 likely benign Limb-Girdle Muscular Dystrophy, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000407720 SCV000431859 likely benign Miyoshi myopathy 2016-06-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000080322 SCV000269059 benign not specified 2015-01-13 criteria provided, single submitter clinical testing c.6321+15C>T in intron 55 of DYSF: This variant is not expected to have clinical significance because it is not located within the conserved splice consensus se quence. It has been identified in 22.9% (1966/8598) of European American chromos omes from a broad population by the NHLBI Exome Sequencing Project (http://evs.g s.washington.edu/EVS; dbSNP rs2559082).
PreventionGenetics RCV000080322 SCV000309703 benign not specified criteria provided, single submitter clinical testing

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