ClinVar Miner

Submissions for variant NM_000231.3(SGCG):c.196-6del

dbSNP: rs568365779
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000363057 SCV000344683 benign not specified 2017-02-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003603049 SCV004561216 benign Autosomal recessive limb-girdle muscular dystrophy type 2C 2025-01-30 criteria provided, single submitter clinical testing

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