ClinVar Miner

Submissions for variant NM_006790.3(MYOT):c.-89del

dbSNP: rs886059966
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000294444 SCV000452976 uncertain significance Limb-Girdle Muscular Dystrophy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV003312996 SCV000452977 uncertain significance Myofibrillar myopathy 3 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000399508 SCV000452978 uncertain significance Myofibrillar Myopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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