List of variants in gene SGCG reported as likely benign by Eurofins NTD LLC (GA)

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.-6T>C	rs141771521	0.00749
NM_000231.3(SGCG):c.832G>A (p.Gly278Ser)	rs147820869	0.00049
NM_000231.3(SGCG):c.196-7_196-6del	rs568365779

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