List of variants in gene GRN reported as likely benign by Illumina Laboratory Services, Illumina

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.384T>C (p.Asp128=)	rs25646	0.02616
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.1297C>T (p.Arg433Trp)	rs63750412	0.00523
NM_002087.4(GRN):c.546G>A (p.Thr182=)	rs138473783	0.00335
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_002087.3(GRN):c.-45C>G	rs563336550	0.00057
NM_002087.4(GRN):c.903G>A (p.Ser301=)	rs63750142	0.00044
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln)	rs63751100	0.00022
NM_002087.4(GRN):c.268G>A (p.Val90Met)	rs200019356	0.00006
NM_002087.4(GRN):c.139-3T>C	rs371119011	0.00002
NM_002087.4(GRN):c.1019A>T (p.His340Leu)	rs775196555	0.00001
NM_002087.4(GRN):c.1357G>A (p.Gly453Arg)	rs751072702	0.00001
NM_002087.4(GRN):c.99C>T (p.Asp33=)	rs63750742

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.