List of variants in gene SGCG reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.539A>T (p.Glu180Val)	rs114160429	0.00101
NM_000231.3(SGCG):c.102C>T (p.Arg34=)	rs140810408	0.00011
NM_000231.3(SGCG):c.345G>A (p.Ala115=)	rs1800352	0.00003
NM_000231.3(SGCG):c.196-7_196-6del	rs568365779
NM_000231.3(SGCG):c.579-15_579-12dup
NM_000231.3(SGCG):c.579-22G>T	rs111358030
NM_000231.3(SGCG):c.579-23T>G
NM_000231.3(SGCG):c.579-23_579-21del
NM_000231.3(SGCG):c.579-24_579-21del
NM_000231.3(SGCG):c.579-24_579-23del
NM_000231.3(SGCG):c.739C>T (p.Leu247=)

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