ClinVar Miner

Submissions for variant NM_000337.6(SGCD):c.383-35_383-34insA

dbSNP: rs1554119750
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000664810 SCV000788825 likely benign Dilated cardiomyopathy 1L; Autosomal recessive limb-girdle muscular dystrophy type 2F 2017-01-06 criteria provided, single submitter clinical testing

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