rs267607515

Orientation

minus

Stabilized

minus

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

Make rs267607515(C;C)

Make rs267607515(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911293

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607515
dbSNP (classic)	rs267607515
ClinGen	rs267607515
ebi	rs267607515
HLI	rs267607515
Exac	rs267607515
Gnomad	rs267607515
Varsome	rs267607515
LitVar	rs267607515
Map	rs267607515
PheGenI	rs267607515
Biobank	rs267607515
1000 genomes	rs267607515
hgdp	rs267607515
ensembl	rs267607515
geneview	rs267607515
scholar	rs267607515
google	rs267607515
pharmgkb	rs267607515
gwascentral	rs267607515
openSNP	rs267607515
23andMe	rs267607515
SNPshot	rs267607515
SNPdbe	rs267607515
MSV3d	rs267607515
GWAS Ctlg	rs267607515

Max Magnitude

0

ClinVar
Risk	rs267607515(A;A) rs267607515(C;C)
Alt	rs267607515(A;A) rs267607515(C;C)
Reference	Rs267607515(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.42988661A>G
CLNSRC
CLNACC	RCV000056821.1, RCV000192157.1,