List of variants in gene SGCD reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.84T>C (p.Tyr28=)	rs1801193	0.39558
NM_000337.5(SGCD):c.-303A>T	rs7725121	0.06375
NM_000337.6(SGCD):c.290G>A (p.Arg97Gln)	rs45559835	0.04292
NM_000337.5(SGCD):c.-179A>G	rs77808502	0.00918
NM_000337.6(SGCD):c.507G>A (p.Ala169=)	rs10071079	0.00680
NM_000337.6(SGCD):c.294+8T>C	rs11748588	0.00640
NM_000337.6(SGCD):c.699+71G>A	rs187204080	0.00245
NM_000337.6(SGCD):c.144G>C (p.Val48=)	rs372152495	0.00106
NM_000337.6(SGCD):c.699+18C>G	rs180898690	0.00019
NM_000337.5(SGCD):c.-372C>G	rs7717393
NM_000337.5(SGCD):c.-412A>T	rs7724969
NM_000337.6(SGCD):c.-94C>G	rs13170573
NM_000337.6(SGCD):c.105G>C (p.Leu35=)	rs193922392
NM_000337.6(SGCD):c.699+13_699+15del	rs397517924

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