"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SGCD"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2682910	NM_000337.6(SGCD):c.3+5G>A	SGCD	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 196255	NM_000337.6(SGCD):c.92G>A (p.Arg31Gln)	SGCD (R31Q +1 more)	Single nucleotide variant (missense variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 3379614	NM_000337.6(SGCD):c.510G>C (p.Glu170Asp)	SGCD (E169D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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