List of variants in gene AGL reported as likely benign by Natera, Inc.

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000642.3(AGL):c.3619G>A (p.Ala1207Thr)	rs11807956	0.00940
NM_000642.3(AGL):c.1885G>A (p.Glu629Lys)	rs146041189	0.00160
NM_000642.3(AGL):c.3431T>A (p.Ile1144Asn)	rs2230308	0.00113
NM_000642.3(AGL):c.1759C>T (p.His587Tyr)	rs139488862	0.00053
NM_000642.3(AGL):c.1908A>G (p.Ser636=)	rs144723143	0.00051
NM_000642.3(AGL):c.4575T>A (p.Ile1525=)	rs372116308	0.00016
NM_000642.3(AGL):c.3231G>A (p.Lys1077=)	rs138063386	0.00011
NM_000642.3(AGL):c.1602C>T (p.His534=)	rs563472929	0.00009
NM_000642.3(AGL):c.174T>C (p.Asn58=)	rs779677453	0.00004
NM_000642.3(AGL):c.3345A>T (p.Gly1115=)	rs758265909	0.00003
NM_000642.3(AGL):c.2574C>T (p.Val858=)	rs772038934	0.00001
NM_000642.3(AGL):c.2497C>A (p.Gln833Lys)	rs757870729

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