List of variants in gene combination SACS, SGCG reported as benign for autosomal recessive limb-girdle muscular dystrophy type 2C

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.860A>G (p.Asn287Ser)	rs1800354	0.83747
NM_000231.3(SGCG):c.705T>C (p.Leu235=)	rs1800353	0.60006
NM_000231.3(SGCG):c.*254G>A	rs3751371	0.31172

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