rs63749877

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CACT;CACT)	0	common in clinvar
(CTCA;CTCA)	0	common in clinvar
(I;I)	0

Make rs63749877(-;-)

Make rs63749877(-;CACT)

Reference

GRCh38 38.1/141

Chromosome

17

Position

44351141

Gene

GRN

is a	snp
is	mentioned by
dbSNP	rs63749877
dbSNP (classic)	rs63749877
ClinGen	rs63749877
ebi	rs63749877
HLI	rs63749877
Exac	rs63749877
Gnomad	rs63749877
Varsome	rs63749877
LitVar	rs63749877
Map	rs63749877
PheGenI	rs63749877
Biobank	rs63749877
1000 genomes	rs63749877
hgdp	rs63749877
ensembl	rs63749877
geneview	rs63749877
scholar	rs63749877
google	rs63749877
pharmgkb	rs63749877
gwascentral	rs63749877
openSNP	rs63749877
23andMe	rs63749877
SNPshot	rs63749877
SNPdbe	rs63749877
MSV3d	rs63749877
GWAS Ctlg	rs63749877

Max Magnitude

0

ClinVar
Risk	rs63749877(-;-)
Alt	rs63749877(-;-)
Reference	Rs63749877(CTCA;CTCA)
Significance	Pathogenic
Disease	Frontotemporal dementia Primary progressive aphasia Ceroid lipofuscinosis not provided
Variation	info
Gene	GRN
CLNDBN	Frontotemporal dementia, ubiquitin-positive Primary progressive aphasia Ceroid lipofuscinosis, neuronal, 11 not provided
Reversed	0
HGVS	NC_000017.10:g.42428509_42428512delCACT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017393.25, RCV000017394.28, RCV000029169.28, RCV000084585.1,