List of variants in gene AGRN reported as benign by Genetic Services Laboratory, University of Chicago

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_198576.4(AGRN):c.1178-6T>C	rs2799066	0.87183
NM_198576.4(AGRN):c.3558T>C (p.Phe1186=)	rs10267	0.81774
NM_198576.4(AGRN):c.3066A>G (p.Ser1022=)	rs2465128	0.79176
NM_198576.4(AGRN):c.5651+5C>T	rs9803031	0.77551
NM_198576.4(AGRN):c.6057C>T (p.Asp2019=)	rs4275402	0.59050
NM_198576.4(AGRN):c.4161T>C (p.Thr1387=)	rs9442391	0.49370
NM_198576.4(AGRN):c.45G>T (p.Pro15=)	rs115173026	0.30662
NM_198576.4(AGRN):c.804C>T (p.Ala268=)	rs113789806	0.04323
NM_198576.4(AGRN):c.5070C>T (p.Phe1690=)	rs17160776	0.04120
NM_198576.4(AGRN):c.2183A>T (p.Glu728Val)	rs113288277	0.02922
NM_198576.4(AGRN):c.1993G>A (p.Glu665Lys)	rs143324306	0.00297
NM_198576.4(AGRN):c.2993C>T (p.Pro998Leu)	rs200807722	0.00036

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