List of variants in gene GRN reported as pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.1252C>T (p.Arg418Ter)	rs63751180
NM_002087.4(GRN):c.25del (p.Ala9fs)	rs2048347685
NM_002087.4(GRN):c.599-2A>G	rs1191556044
NM_002087.4(GRN):c.675_676del (p.Ser226fs)	rs63751085
NM_002087.4(GRN):c.78C>A (p.Cys26Ter)	rs2143325486

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