List of variants in gene SGCD reported as benign by Eurofins NTD LLC (GA)

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.84T>C (p.Tyr28=)	rs1801193	0.39558
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.295-40T>A	rs74571343	0.01950
NM_000337.6(SGCD):c.294+8T>C	rs11748588	0.00640
NM_000337.6(SGCD):c.699+71G>A	rs187204080	0.00245
NM_000337.6(SGCD):c.*2A>C	rs200757725	0.00241
NM_000337.6(SGCD):c.15G>C (p.Glu5Asp)	rs549319429	0.00004
NM_000337.6(SGCD):c.699+13_699+15del	rs397517924

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