List of variants in gene GRN reported as benign by GeneDx

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.-8+50dup	rs11398947	0.99993
NM_002087.4(GRN):c.*78C>T	rs5848	0.41298
NM_002087.4(GRN):c.462+24G>A	rs850713	0.27231
NM_002087.4(GRN):c.264+21G>A	rs9897526	0.19972
NM_002087.4(GRN):c.835+7G>A	rs72824736	0.04753
NM_002087.4(GRN):c.384T>C (p.Asp128=)	rs25646	0.02616
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.1297C>T (p.Arg433Trp)	rs63750412	0.00523
NM_002087.4(GRN):c.-7-320C>G	rs78403836
NM_002087.4(GRN):c.350-50_350-47dup	rs34424835

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