List of variants in gene SDCCAG8 reported as likely benign by Genetic Services Laboratory, University of Chicago

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_006642.5(SDCCAG8):c.279G>A (p.Pro93=)	rs145877279	0.00120
NM_006642.5(SDCCAG8):c.267T>C (p.Ser89=)	rs148818431	0.00069
NM_006642.5(SDCCAG8):c.1094G>A (p.Arg365Lys)	rs115098969
NM_006642.5(SDCCAG8):c.1094G>C (p.Arg365Thr)	rs115098969
NM_006642.5(SDCCAG8):c.597C>T (p.Gly199=)	rs143407309

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