List of variants in gene GRN reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.264+7G>A	rs60100877	0.00548
NM_002087.4(GRN):c.-14G>C	rs1237619973
NM_002087.4(GRN):c.828G>T (p.Ala276=)	rs761530797

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