rs267607502

Orientation

minus

Stabilized

minus

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

Make rs267607502(A;G)

Make rs267607502(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911266

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607502
dbSNP (classic)	rs267607502
ClinGen	rs267607502
ebi	rs267607502
HLI	rs267607502
Exac	rs267607502
Gnomad	rs267607502
Varsome	rs267607502
LitVar	rs267607502
Map	rs267607502
PheGenI	rs267607502
Biobank	rs267607502
1000 genomes	rs267607502
hgdp	rs267607502
ensembl	rs267607502
geneview	rs267607502
scholar	rs267607502
google	rs267607502
pharmgkb	rs267607502
gwascentral	rs267607502
openSNP	rs267607502
23andMe	rs267607502
SNPshot	rs267607502
SNPdbe	rs267607502
MSV3d	rs267607502
GWAS Ctlg	rs267607502

Max Magnitude

0

ClinVar
Risk	rs267607502(G;G)
Alt	rs267607502(G;G)
Reference	Rs267607502(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.42988634T>C
CLNSRC
CLNACC	RCV000056829.1, RCV000192168.1,