rs267607503

Orientation

minus

Stabilized

minus

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

Make rs267607503(C;T)

Make rs267607503(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911272

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607503
dbSNP (classic)	rs267607503
ClinGen	rs267607503
ebi	rs267607503
HLI	rs267607503
Exac	rs267607503
Gnomad	rs267607503
Varsome	rs267607503
LitVar	rs267607503
Map	rs267607503
PheGenI	rs267607503
Biobank	rs267607503
1000 genomes	rs267607503
hgdp	rs267607503
ensembl	rs267607503
geneview	rs267607503
scholar	rs267607503
google	rs267607503
pharmgkb	rs267607503
gwascentral	rs267607503
openSNP	rs267607503
23andMe	rs267607503
SNPshot	rs267607503
SNPdbe	rs267607503
MSV3d	rs267607503
GWAS Ctlg	rs267607503

Max Magnitude

0

ClinVar
Risk	rs267607503(T;T)
Alt	rs267607503(T;T)
Reference	Rs267607503(C;C)
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.42988640G>A
CLNSRC
CLNACC	RCV000056827.1, RCV000192166.1,