List of variants in gene SGCD reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.290G>A (p.Arg97Gln)	rs45559835	0.04292
NM_000337.6(SGCD):c.700-19T>C	rs80086857	0.02231
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+13_699+15del	rs397517924

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