rs267607523

Orientation

minus

Stabilized

minus

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

Make rs267607523(A;A)

Make rs267607523(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44915273

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607523
dbSNP (classic)	rs267607523
ClinGen	rs267607523
ebi	rs267607523
HLI	rs267607523
Exac	rs267607523
Gnomad	rs267607523
Varsome	rs267607523
LitVar	rs267607523
Map	rs267607523
PheGenI	rs267607523
Biobank	rs267607523
1000 genomes	rs267607523
hgdp	rs267607523
ensembl	rs267607523
geneview	rs267607523
scholar	rs267607523
google	rs267607523
pharmgkb	rs267607523
gwascentral	rs267607523
openSNP	rs267607523
23andMe	rs267607523
SNPshot	rs267607523
SNPdbe	rs267607523
MSV3d	rs267607523
GWAS Ctlg	rs267607523

Max Magnitude

0

ClinVar
Risk	rs267607523(A;A)
Alt	rs267607523(A;A)
Reference	Rs267607523(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.42992641C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056858.1, RCV000192101.1,