List of variants in gene AGL reported as benign by Eurofins NTD LLC (GA)

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_000642.3(AGL):c.894C>T (p.Leu298=)	rs2230306	0.76251
NM_000642.3(AGL):c.-10A>G	rs2307130	0.41188
NM_000642.3(AGL):c.112A>G (p.Thr38Ala)	rs35278779	0.01527
NM_000642.3(AGL):c.1160G>A (p.Arg387Gln)	rs17121464	0.01447
NM_000642.3(AGL):c.1481G>A (p.Arg494His)	rs141043166	0.00743
NM_000642.3(AGL):c.3203A>G (p.Tyr1068Cys)	rs147165298	0.00193

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