rs267607506

Orientation

minus

Stabilized

minus

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

Make rs267607506(C;C)

Make rs267607506(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44915240

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607506
dbSNP (classic)	rs267607506
ClinGen	rs267607506
ebi	rs267607506
HLI	rs267607506
Exac	rs267607506
Gnomad	rs267607506
Varsome	rs267607506
LitVar	rs267607506
Map	rs267607506
PheGenI	rs267607506
Biobank	rs267607506
1000 genomes	rs267607506
hgdp	rs267607506
ensembl	rs267607506
geneview	rs267607506
scholar	rs267607506
google	rs267607506
pharmgkb	rs267607506
gwascentral	rs267607506
openSNP	rs267607506
23andMe	rs267607506
SNPshot	rs267607506
SNPdbe	rs267607506
MSV3d	rs267607506
GWAS Ctlg	rs267607506

Max Magnitude

0

ClinVar
Risk	rs267607506(A;A) rs267607506(C;C)
Alt	rs267607506(A;A) rs267607506(C;C)
Reference	Rs267607506(T;T)
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.42992608A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056872.1, RCV000192114.1,