List of variants in gene SGCA reported as benign for not specified

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_000023.4(SGCA):c.*6T>C	rs2696288	0.91073
NM_000023.4(SGCA):c.313-39C>A	rs59944537	0.14899
NM_000023.4(SGCA):c.933C>T (p.Val311=)	rs1801191	0.08920
NM_000023.4(SGCA):c.528C>T (p.Thr176=)	rs1801190	0.00912
NM_000023.4(SGCA):c.*10C>G	rs60300808	0.00619
NM_000023.4(SGCA):c.1120C>T (p.Arg374Cys)	rs35495899	0.00555
NM_000023.4(SGCA):c.-8G>A	rs149296410	0.00248
NM_000023.4(SGCA):c.329G>A (p.Arg110Gln)	rs145697858	0.00087
NM_000023.4(SGCA):c.38-46G>C	rs142537375
NM_000023.4(SGCA):c.747+21C>T

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