List of variants in gene ALG13 reported as likely benign by Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)

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_001099922.3(ALG13):c.2672C>T (p.Ser891Phe)	rs200066623	0.00390
NM_001099922.3(ALG13):c.2248-4A>G	rs370438099	0.00325
NM_001099922.3(ALG13):c.1834C>T (p.Pro612Ser)	rs200516126	0.00009
NM_001099922.3(ALG13):c.2380GAA[1] (p.Glu795del)	rs772766102

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