rs267607525

Orientation

minus

Stabilized

minus

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

Make rs267607525(A;C)

Make rs267607525(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44913342

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607525
dbSNP (classic)	rs267607525
ClinGen	rs267607525
ebi	rs267607525
HLI	rs267607525
Exac	rs267607525
Gnomad	rs267607525
Varsome	rs267607525
LitVar	rs267607525
Map	rs267607525
PheGenI	rs267607525
Biobank	rs267607525
1000 genomes	rs267607525
hgdp	rs267607525
ensembl	rs267607525
geneview	rs267607525
scholar	rs267607525
google	rs267607525
pharmgkb	rs267607525
gwascentral	rs267607525
openSNP	rs267607525
23andMe	rs267607525
SNPshot	rs267607525
SNPdbe	rs267607525
MSV3d	rs267607525
GWAS Ctlg	rs267607525

Max Magnitude

0

ClinVar
Risk	rs267607525(C;C)
Alt	rs267607525(C;C)
Reference	Rs267607525(A;A)
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.42990710T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056897.1, RCV000192134.1,