List of variants in gene GRN reported as benign

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: 37

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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.-8+46G>T	rs564341543	0.19681
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.*280G>A	rs116547342	0.01005
NM_002087.4(GRN):c.1544G>C (p.Gly515Ala)	rs25647	0.00781
NM_002087.3(GRN):c.-72G>T	rs76783532	0.00635
NM_002087.4(GRN):c.264+7G>A	rs60100877	0.00548
NM_002087.4(GRN):c.42G>A (p.Leu14=)	rs111435385	0.00533
NM_002087.4(GRN):c.1297C>T (p.Arg433Trp)	rs63750412	0.00523
NM_002087.4(GRN):c.545C>T (p.Thr182Met)	rs63750479	0.00356
NM_002087.4(GRN):c.546G>A (p.Thr182=)	rs138473783	0.00335
NM_002087.4(GRN):c.1227G>A (p.Thr409=)	rs140298583	0.00326
NM_002087.4(GRN):c.-38T>C	rs530686556	0.00325
NM_002087.4(GRN):c.1298G>A (p.Arg433Gln)	rs114248177	0.00247
NM_002087.4(GRN):c.970G>A (p.Ala324Thr)	rs63750541	0.00112
NM_002087.4(GRN):c.228C>T (p.Thr76=)	rs144736470	0.00086
NM_002087.4(GRN):c.359C>A (p.Ser120Tyr)	rs63750043	0.00076
NM_002087.4(GRN):c.253C>G (p.Pro85Ala)	rs143560849	0.00058
NM_002087.4(GRN):c.393C>G (p.Phe131Leu)	rs149180605	0.00052
NM_002087.4(GRN):c.903G>A (p.Ser301=)	rs63750142	0.00044
NM_002087.3(GRN):c.-56T>G	rs909307115	0.00032
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln)	rs63751100	0.00022
NM_002087.4(GRN):c.626C>T (p.Pro209Leu)	rs368995988	0.00008
NM_002087.4(GRN):c.1742A>T (p.Asp581Val)	rs768223928	0.00007
NM_002087.4(GRN):c.267C>T (p.Ala89=)	rs201699327	0.00001
NM_002087.4(GRN):c.-7-320C>G	rs78403836
NM_002087.4(GRN):c.1180-3del
NM_002087.4(GRN):c.350-50_350-47dup	rs34424835
NM_002087.4(GRN):c.414G>C (p.Thr138=)	rs543344476
NM_002087.4(GRN):c.463-6dup	rs780699082
NM_002087.4(GRN):c.933+11del
NM_002087.4(GRN):c.99C>T (p.Asp33=)	rs63750742

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