ClinVar Miner

Submissions for variant NM_000337.5(SGCD):c.-43-1G>A (rs767016855)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section,National Institutes of Health RCV000172103 SCV000055142 uncertain significance not provided 2013-06-24 criteria provided, single submitter research
Counsyl RCV000671293 SCV000796254 uncertain significance Dilated cardiomyopathy 1L; Autosomal recessive limb-girdle muscular dystrophy type 2F 2017-12-08 criteria provided, single submitter clinical testing

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