rs267607514

Orientation

minus

Stabilized

minus

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

Make rs267607514(A;A)

Make rs267607514(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911369

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607514
dbSNP (classic)	rs267607514
ClinGen	rs267607514
ebi	rs267607514
HLI	rs267607514
Exac	rs267607514
Gnomad	rs267607514
Varsome	rs267607514
LitVar	rs267607514
Map	rs267607514
PheGenI	rs267607514
Biobank	rs267607514
1000 genomes	rs267607514
hgdp	rs267607514
ensembl	rs267607514
geneview	rs267607514
scholar	rs267607514
google	rs267607514
pharmgkb	rs267607514
gwascentral	rs267607514
openSNP	rs267607514
23andMe	rs267607514
SNPshot	rs267607514
SNPdbe	rs267607514
MSV3d	rs267607514
GWAS Ctlg	rs267607514

Max Magnitude

0

ClinVar
Risk	rs267607514(A;A)
Alt	rs267607514(A;A)
Reference	Rs267607514(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.42988737C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056919.1, RCV000192152.1, RCV000192154.1,