ClinVar Miner

Submissions for variant NM_000337.5(SGCD):c.383-33CTCTCTAT[4] (rs727504998)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000367765 SCV000341231 uncertain significance not provided 2016-04-15 criteria provided, single submitter clinical testing
Counsyl RCV000664732 SCV000788739 uncertain significance Dilated cardiomyopathy 1L; Autosomal recessive limb-girdle muscular dystrophy type 2F 2017-01-05 criteria provided, single submitter clinical testing

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