List of variants in gene AGL reported as 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_000642.3(AGL):c.1155G>T (p.Lys385Asn)	rs28730701	0.01764
NM_000642.3(AGL):c.112A>G (p.Thr38Ala)	rs35278779	0.01527
NM_000642.3(AGL):c.3849T>C (p.Ala1283=)	rs28730706	0.01312
NM_000642.3(AGL):c.*2058G>A	rs12117747	0.00930

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