rs267607511

Orientation

minus

Stabilized

minus

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

Make rs267607511(C;C)

Make rs267607511(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911287

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607511
dbSNP (classic)	rs267607511
ClinGen	rs267607511
ebi	rs267607511
HLI	rs267607511
Exac	rs267607511
Gnomad	rs267607511
Varsome	rs267607511
LitVar	rs267607511
Map	rs267607511
PheGenI	rs267607511
Biobank	rs267607511
1000 genomes	rs267607511
hgdp	rs267607511
ensembl	rs267607511
geneview	rs267607511
scholar	rs267607511
google	rs267607511
pharmgkb	rs267607511
gwascentral	rs267607511
openSNP	rs267607511
23andMe	rs267607511
SNPshot	rs267607511
SNPdbe	rs267607511
MSV3d	rs267607511
GWAS Ctlg	rs267607511

Max Magnitude

0

ClinVar
Risk	rs267607511(C;C)
Alt	rs267607511(C;C)
Reference	Rs267607511(T;T)
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.42988655A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056823.1, RCV000192161.1,