rs267607510

Orientation

minus

Stabilized

minus

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

Make rs267607510(A;A)

Make rs267607510(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44915278

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607510
dbSNP (classic)	rs267607510
ClinGen	rs267607510
ebi	rs267607510
HLI	rs267607510
Exac	rs267607510
Gnomad	rs267607510
Varsome	rs267607510
LitVar	rs267607510
Map	rs267607510
PheGenI	rs267607510
Biobank	rs267607510
1000 genomes	rs267607510
hgdp	rs267607510
ensembl	rs267607510
geneview	rs267607510
scholar	rs267607510
google	rs267607510
pharmgkb	rs267607510
gwascentral	rs267607510
openSNP	rs267607510
23andMe	rs267607510
SNPshot	rs267607510
SNPdbe	rs267607510
MSV3d	rs267607510
GWAS Ctlg	rs267607510

Max Magnitude

0

ClinVar
Risk	rs267607510(A;A)
Alt	rs267607510(A;A)
Reference	Rs267607510(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.42992646C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056856.1, RCV000192099.1,