ClinVar Miner

Submissions for variant NM_000337.6(SGCD):c.*4341dup

dbSNP: rs556887176
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000325403 SCV000455653 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000382359 SCV000455654 uncertain significance Limb-girdle muscular dystrophy, recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000294484 SCV000455655 uncertain significance Qualitative or quantitative defects of delta-sarcoglycan 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695850 SCV005188711 uncertain significance not provided criteria provided, single submitter not provided

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