List of variants in gene AGRN reported as uncertain significance for not specified

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.67G>C (p.Val23Leu)	rs201073369	0.00583
NM_198576.4(AGRN):c.4639G>A (p.Glu1547Lys)	rs2799068	0.00284
NM_198576.4(AGRN):c.1570C>T (p.Arg524Trp)	rs144164397	0.00119
NM_198576.4(AGRN):c.3732C>T (p.His1244=)	rs536657086	0.00017
NM_198576.4(AGRN):c.2559C>T (p.Gly853=)	rs369198471	0.00007
NM_198576.4(AGRN):c.2473C>T (p.Arg825Cys)	rs370387335	0.00006
NM_198576.4(AGRN):c.526C>T (p.Leu176=)	rs544749044	0.00005
NM_198576.4(AGRN):c.3752-6C>T	rs779516004	0.00004
NM_198576.4(AGRN):c.1978C>T (p.Arg660Trp)	rs534519250	0.00001
NM_198576.4(AGRN):c.3856C>A (p.Pro1286Thr)	rs760218476	0.00001
NM_198576.4(AGRN):c.4587C>A (p.Arg1529=)	rs2100677874
NM_198576.4(AGRN):c.5332G>A (p.Ala1778Thr)	rs538792693

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