List of variants in gene SGCD reported as benign for Limb-Girdle Muscular Dystrophy, Recessive

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.*6717G>A	rs1827368	0.90216
NM_000337.6(SGCD):c.84T>C (p.Tyr28=)	rs1801193	0.39558
NM_000337.6(SGCD):c.*1527C>T	rs284445	0.26081
NM_000337.6(SGCD):c.*3772dup	rs397841758	0.20069
NM_000337.6(SGCD):c.*5863C>T	rs11953631	0.15411
NM_000337.6(SGCD):c.*4395A>T	rs10041876	0.15385
NM_000337.6(SGCD):c.*781G>C	rs3857412	0.14424
NM_000337.6(SGCD):c.*1618T>C	rs1389818	0.14033
NM_000337.6(SGCD):c.*4813T>C	rs1845479	0.14018
NM_000337.6(SGCD):c.-94C>G	rs13170573

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