List of variants in gene SDCCAG8 reported as uncertain significance by GeneDx

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006642.5(SDCCAG8):c.1501G>C (p.Asp501His)	rs150646039	0.00138
NM_006642.5(SDCCAG8):c.572C>T (p.Thr191Ile)	rs150070966	0.00088
NM_006642.5(SDCCAG8):c.1276A>G (p.Thr426Ala)	rs201580075	0.00029
NM_006642.5(SDCCAG8):c.1525C>G (p.Gln509Glu)	rs199919586	0.00023
NM_006642.5(SDCCAG8):c.244C>T (p.Arg82Cys)	rs143447584	0.00009
NM_006642.5(SDCCAG8):c.968G>A (p.Arg323Lys)	rs576672580	0.00005
NM_006642.5(SDCCAG8):c.1375T>C (p.Tyr459His)	rs1182496392	0.00003
NM_006642.5(SDCCAG8):c.1064C>A (p.Thr355Asn)	rs199524638	0.00001
NM_006642.5(SDCCAG8):c.1273G>T (p.Val425Phe)	rs370072966
NM_006642.5(SDCCAG8):c.1356G>A (p.Lys452=)	rs1057515483

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