List of variants in gene SGCD reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.294+8T>C	rs11748588	0.00640
NM_000337.6(SGCD):c.510G>A (p.Glu170=)	rs368838376	0.00029
NM_000337.6(SGCD):c.105G>C (p.Leu35=)	rs193922392
NM_000337.6(SGCD):c.516A>G (p.Thr172=)	rs753952200

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