rs63749801

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGTC;AGTC)	0	common in clinvar
(CAGT;CAGT)	0	common in clinvar
(I;I)	0

Make rs63749801(-;-)

Make rs63749801(-;CAGT)

Reference

GRCh38 38.1/142

Chromosome

17

Position

44350266

Gene

GRN

is a	snp
is	mentioned by
dbSNP	rs63749801
dbSNP (classic)	rs63749801
ClinGen	rs63749801
ebi	rs63749801
HLI	rs63749801
Exac	rs63749801
Gnomad	rs63749801
Varsome	rs63749801
LitVar	rs63749801
Map	rs63749801
PheGenI	rs63749801
Biobank	rs63749801
1000 genomes	rs63749801
hgdp	rs63749801
ensembl	rs63749801
geneview	rs63749801
scholar	rs63749801
google	rs63749801
pharmgkb	rs63749801
gwascentral	rs63749801
openSNP	rs63749801
23andMe	rs63749801
SNPshot	rs63749801
SNPdbe	rs63749801
MSV3d	rs63749801
GWAS Ctlg	rs63749801

Max Magnitude

0

ClinVar
Risk	rs63749801(-;-) Rs63749801(AGTC;AGTC)
Alt	rs63749801(-;-) Rs63749801(AGTC;AGTC)
Reference	Rs63749801(CAGT;CAGT)
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.42427634_42427637delCAGT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017384.28, RCV000084442.1,