Variants in gene GRN with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.55C>T (p.Arg19Trp)	rs63750723	0.01303
NM_002087.4(GRN):c.1544G>C (p.Gly515Ala)	rs25647	0.00781
NM_002087.4(GRN):c.264+7G>A	rs60100877	0.00548
NM_002087.4(GRN):c.1297C>T (p.Arg433Trp)	rs63750412	0.00523
NM_002087.4(GRN):c.545C>T (p.Thr182Met)	rs63750479	0.00356
NM_002087.4(GRN):c.546G>A (p.Thr182=)	rs138473783	0.00335
NM_002087.4(GRN):c.1227G>A (p.Thr409=)	rs140298583	0.00326
NM_002087.4(GRN):c.970G>A (p.Ala324Thr)	rs63750541	0.00112
NM_002087.4(GRN):c.228C>T (p.Thr76=)	rs144736470	0.00086
NM_002087.4(GRN):c.359C>A (p.Ser120Tyr)	rs63750043	0.00076
NM_002087.4(GRN):c.253C>G (p.Pro85Ala)	rs143560849	0.00058
NM_002087.4(GRN):c.903G>A (p.Ser301=)	rs63750142	0.00044
NM_002087.4(GRN):c.1742A>T (p.Asp581Val)	rs768223928	0.00007
NM_002087.4(GRN):c.99C>T (p.Asp33=)	rs63750742

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