List of variants in gene SGCD reported as pathogenic for not provided

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.4-1G>A	rs1554094927	0.00001
NM_000337.6(SGCD):c.493C>T (p.Arg165Ter)	rs121909295	0.00001
NM_000337.6(SGCD):c.443T>A (p.Leu148Ter)	rs886043460
NM_000337.6(SGCD):c.65dup (p.Tyr23fs)	rs886043031
NM_000337.6(SGCD):c.97C>T (p.Arg33Ter)	rs778760498

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