List of variants in gene AGL reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000642.3(AGL):c.2390A>G (p.Asn797Ser)	rs149210307	0.00212
NM_000642.3(AGL):c.1885G>A (p.Glu629Lys)	rs146041189	0.00160
NM_000642.3(AGL):c.1810T>G (p.Phe604Val)	rs138105395	0.00125
NM_000642.3(AGL):c.968G>A (p.Arg323Gln)	rs139399527	0.00123
NM_000642.3(AGL):c.1759C>T (p.His587Tyr)	rs139488862	0.00053
NM_000642.3(AGL):c.1028G>A (p.Arg343Gln)	rs137943515	0.00047
NM_000642.3(AGL):c.767G>A (p.Arg256His)	rs200180652	0.00004
NM_000642.3(AGL):c.4186A>G (p.Lys1396Glu)	rs539403694	0.00002

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