rs63751006

Orientation

plus

Stabilized

plus

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

Make rs63751006(C;C)

Make rs63751006(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

44349166

Gene

GRN

is a	snp
is	mentioned by
dbSNP	rs63751006
dbSNP (classic)	rs63751006
ClinGen	rs63751006
ebi	rs63751006
HLI	rs63751006
Exac	rs63751006
Gnomad	rs63751006
Varsome	rs63751006
LitVar	rs63751006
Map	rs63751006
PheGenI	rs63751006
Biobank	rs63751006
1000 genomes	rs63751006
hgdp	rs63751006
ensembl	rs63751006
geneview	rs63751006
scholar	rs63751006
google	rs63751006
pharmgkb	rs63751006
gwascentral	rs63751006
openSNP	rs63751006
23andMe	rs63751006
SNPshot	rs63751006
SNPdbe	rs63751006
MSV3d	rs63751006
GWAS Ctlg	rs63751006

Max Magnitude

0

OMIM	138945
Desc
Variant	0003
Related	also

ClinVar
Risk	rs63751006(C;C)
Alt	rs63751006(C;C)
Reference	Rs63751006(T;T)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	GRN
CLNDBN	Frontotemporal dementia, ubiquitin-positive not provided
Reversed	0
HGVS	NC_000017.10:g.42426534T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017381.27, RCV000084419.1,