"Revvity Omics, Revvity"[submitter] AND "GRN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1324516	NM_002087.4(GRN):c.139-2A>G	GRN	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 1506670	NM_002087.4(GRN):c.361G>A (p.Val121Met)	GRN (V121M)	Single nucleotide variant (missense variant)	GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +2 more	GUncertain significance
Select item 2137052	NM_002087.4(GRN):c.406T>G (p.Phe136Val)	GRN (F136V)	Single nucleotide variant (missense variant)	Neuronal ceroid lipofuscinosis 11 +2 more	GUncertain significance
Select item 203460	NM_002087.4(GRN):c.708+1G>A	GRN, LOC125177489	Single nucleotide variant (splice donor variant)	GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +2 more	GPathogenic/Likely pathogenic
Select item 1387314	NM_002087.4(GRN):c.796G>C (p.Ala266Pro)	GRN (A266P)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 98170	NM_002087.4(GRN):c.1145del (p.Thr382fs)	GRN (T382fs)	Deletion (frameshift variant)	not provided +2 more	GPathogenic

ClinVar