List of variants in gene ALG3 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_005787.6(ALG3):c.222C>T (p.Tyr74=)	rs200875721	0.00056
NM_005787.6(ALG3):c.669C>T (p.Leu223=)	rs146607327	0.00034
NM_005787.6(ALG3):c.294T>A (p.Leu98=)	rs200538695	0.00001
NM_005787.6(ALG3):c.849C>T (p.Leu283=)

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