rs63750077

Orientation

plus

Stabilized

plus

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

Make rs63750077(C;T)

Make rs63750077(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

44350251

Gene

GRN

is a	snp
is	mentioned by
dbSNP	rs63750077
dbSNP (classic)	rs63750077
ClinGen	rs63750077
ebi	rs63750077
HLI	rs63750077
Exac	rs63750077
Gnomad	rs63750077
Varsome	rs63750077
LitVar	rs63750077
Map	rs63750077
PheGenI	rs63750077
Biobank	rs63750077
1000 genomes	rs63750077
hgdp	rs63750077
ensembl	rs63750077
geneview	rs63750077
scholar	rs63750077
google	rs63750077
pharmgkb	rs63750077
gwascentral	rs63750077
openSNP	rs63750077
23andMe	rs63750077
SNPshot	rs63750077
SNPdbe	rs63750077
MSV3d	rs63750077
GWAS Ctlg	rs63750077

Max Magnitude

0

OMIM	138945
Desc
Variant	0002
Related	also

ClinVar
Risk	rs63750077(T;T)
Alt	rs63750077(T;T)
Reference	Rs63750077(C;C)
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.42427619C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017380.27, RCV000084439.1,