ClinVar Miner

List of variants in gene SGCD reported as likely benign for Dilated Cardiomyopathy, Dominant

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.1846_1847dup	rs527436848	0.00258

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