rs267607521

Orientation

minus

Stabilized

minus

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

Make rs267607521(A;T)

Make rs267607521(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44907369

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607521
dbSNP (classic)	rs267607521
ClinGen	rs267607521
ebi	rs267607521
HLI	rs267607521
Exac	rs267607521
Gnomad	rs267607521
Varsome	rs267607521
LitVar	rs267607521
Map	rs267607521
PheGenI	rs267607521
Biobank	rs267607521
1000 genomes	rs267607521
hgdp	rs267607521
ensembl	rs267607521
geneview	rs267607521
scholar	rs267607521
google	rs267607521
pharmgkb	rs267607521
gwascentral	rs267607521
openSNP	rs267607521
23andMe	rs267607521
SNPshot	rs267607521
SNPdbe	rs267607521
MSV3d	rs267607521
GWAS Ctlg	rs267607521

Max Magnitude

0

ClinVar
Risk	rs267607521(T;T)
Alt	rs267607521(T;T)
Reference	Rs267607521(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.42984737T>A
CLNSRC
CLNACC	RCV000056851.1, RCV000192188.1,