List of variants in gene SGCD reported as uncertain significance 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)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.*1171C>A	rs528794571	0.00003
NM_000337.6(SGCD):c.475G>A (p.Val159Ile)	rs370327314	0.00001
NM_000337.6(SGCD):c.3918_3921dup	rs886060303
NM_000337.6(SGCD):c.4340_4341dup	rs556887176
NM_000337.6(SGCD):c.*4341dup	rs556887176
NM_000337.6(SGCD):c.*6045A>G	rs886060312
NM_000337.6(SGCD):c.*6497dup	rs886060314
NM_000337.6(SGCD):c.*6644del	rs886060315
NM_000337.6(SGCD):c.*6660del	rs57240389
NM_000337.6(SGCD):c.*6660dup	rs57240389
NM_000337.6(SGCD):c.*6661del	rs886060317
NM_000337.6(SGCD):c.8113_8114dup	rs397736317
NM_000337.6(SGCD):c.*8114dup	rs397736317

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