ClinVar Miner

Submissions for variant NM_000337.5(SGCD):c.-626_-616del

dbSNP: rs149976574
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672624 SCV000797746 benign Dilated cardiomyopathy 1L; Autosomal recessive limb-girdle muscular dystrophy type 2F 2018-02-08 criteria provided, single submitter clinical testing
GeneDx RCV001805795 SCV002050375 likely benign not provided 2021-05-26 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003233804 SCV003931727 benign Autosomal recessive limb-girdle muscular dystrophy type 2F 2023-02-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003233805 SCV003931728 benign Dilated cardiomyopathy 1L 2023-02-08 criteria provided, single submitter clinical testing

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