List of variants in gene combination GRN, LOC125177489 reported as pathogenic for hereditary dementia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.708+1G>A	rs63749817	0.00001
NM_002087.4(GRN):c.708+1G>C	rs63749817
NM_002087.4(GRN):c.708+6_708+9del	rs778599933
NM_002087.4(GRN):c.709-1G>A	rs2143337085
NM_002087.4(GRN):c.709-2A>G	rs63750548
NM_002087.4(GRN):c.709-4_713del	rs1598364296
NM_002087.4(GRN):c.711del (p.Thr238fs)

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