rs63749817

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs63749817(A;A)

Make rs63749817(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44350801

Gene

GRN

is a	snp
is	mentioned by
dbSNP	rs63749817
dbSNP (classic)	rs63749817
ClinGen	rs63749817
ebi	rs63749817
HLI	rs63749817
Exac	rs63749817
Gnomad	rs63749817
Varsome	rs63749817
LitVar	rs63749817
Map	rs63749817
PheGenI	rs63749817
Biobank	rs63749817
1000 genomes	rs63749817
hgdp	rs63749817
ensembl	rs63749817
geneview	rs63749817
scholar	rs63749817
google	rs63749817
pharmgkb	rs63749817
gwascentral	rs63749817
openSNP	rs63749817
23andMe	rs63749817
SNPshot	rs63749817
SNPdbe	rs63749817
MSV3d	rs63749817
GWAS Ctlg	rs63749817

Max Magnitude

0

ClinVar
Risk	rs63749817(A;A) rs63749817(C;C)
Alt	rs63749817(A;A) rs63749817(C;C)
Reference	Rs63749817(G;G)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	GRN
CLNDBN	Frontotemporal dementia not provided
Reversed	0
HGVS	NC_000017.10:g.42428169G>A; NC_000017.10:g.42428169G>C
CLNSRC
CLNACC	RCV000185615.1, RCV000084452.1,