List of variants in gene SGCD reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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HGVS	dbSNP	gnomAD frequency
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.213G>A (p.Arg71=)	rs74846539	0.00115
NM_000337.6(SGCD):c.144G>C (p.Val48=)	rs372152495	0.00106
NM_000337.6(SGCD):c.3+20G>A	rs187786098	0.00013
NM_000337.6(SGCD):c.402T>C (p.Ala134=)	rs190935424	0.00007
NM_000337.6(SGCD):c.295-20C>A	rs144250417	0.00006
NM_000337.6(SGCD):c.105G>C (p.Leu35=)	rs193922392
NM_000337.6(SGCD):c.3+19C>T	rs182715924
NM_000337.6(SGCD):c.383-33CTCTCTAT[2]	rs727504998
NM_000337.6(SGCD):c.383-33CTCTCTAT[4]	rs727504998
NM_000337.6(SGCD):c.699+13_699+15del	rs397517924

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