List of variants in gene SGCB reported as likely benign for Autosomal recessive limb-girdle muscular dystrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000232.5(SGCB):c.519G>A (p.Pro173=)	rs755701680	0.00005
NM_000232.5(SGCB):c.282A>G (p.Pro94=)	rs746957769	0.00004
NM_000232.5(SGCB):c.744G>A (p.Glu248=)	rs778608103	0.00004
NM_000232.5(SGCB):c.249A>G (p.Thr83=)	rs565862702	0.00003
NM_000232.5(SGCB):c.390G>A (p.Arg130=)	rs781679527	0.00001

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