rs267607526

Orientation

minus

Stabilized

minus

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

Make rs267607526(C;C)

Make rs267607526(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911252

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607526
dbSNP (classic)	rs267607526
ClinGen	rs267607526
ebi	rs267607526
HLI	rs267607526
Exac	rs267607526
Gnomad	rs267607526
Varsome	rs267607526
LitVar	rs267607526
Map	rs267607526
PheGenI	rs267607526
Biobank	rs267607526
1000 genomes	rs267607526
hgdp	rs267607526
ensembl	rs267607526
geneview	rs267607526
scholar	rs267607526
google	rs267607526
pharmgkb	rs267607526
gwascentral	rs267607526
openSNP	rs267607526
23andMe	rs267607526
SNPshot	rs267607526
SNPdbe	rs267607526
MSV3d	rs267607526
GWAS Ctlg	rs267607526

Max Magnitude

0

ClinVar
Risk	rs267607526(C;C)
Alt	rs267607526(C;C)
Reference	Rs267607526(G;G)
Significance	Pathogenic
Disease	not provided Alexander's disease
Variation	info
Gene	GFAP
CLNDBN	not provided Alexander's disease
Reversed	1
HGVS	NC_000017.10:g.42988620C>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056830.1, RCV000192169.1,