List of variants in gene ALG8 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024079.5(ALG8):c.96-6G>C	rs199911532	0.00160
NM_024079.5(ALG8):c.869A>G (p.Asn290Ser)	rs61995923	0.00050
NC_000011.10:g.78095346G>T
NM_024079.5(ALG8):c.1401G>T (p.Leu467=)
NM_024079.5(ALG8):c.547-319T>C
NM_024079.5(ALG8):c.990C>T (p.Pro330=)

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