List of variants in gene SGCD reported as likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.*2A>C	rs200757725	0.00241
NM_000337.6(SGCD):c.213G>A (p.Arg71=)	rs74846539	0.00115
NM_000337.6(SGCD):c.848A>G (p.Gln283Arg)	rs397516338	0.00019
NM_000337.6(SGCD):c.123C>G (p.Leu41=)	rs200670993	0.00015
NM_000337.6(SGCD):c.394G>A (p.Val132Ile)	rs367819390	0.00010
NM_000337.6(SGCD):c.69C>T (p.Tyr23=)	rs397517923	0.00006
NM_000337.6(SGCD):c.393C>T (p.Ala131=)	rs397517922	0.00004
NM_000337.6(SGCD):c.45T>A (p.Pro15=)	rs727505092	0.00001
NM_000337.6(SGCD):c.177C>T (p.Val59=)	rs727505265

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