rs267607504

Orientation

minus

Stabilized

minus

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

Make rs267607504(C;C)

Make rs267607504(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44915266

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607504
dbSNP (classic)	rs267607504
ClinGen	rs267607504
ebi	rs267607504
HLI	rs267607504
Exac	rs267607504
Gnomad	rs267607504
Varsome	rs267607504
LitVar	rs267607504
Map	rs267607504
PheGenI	rs267607504
Biobank	rs267607504
1000 genomes	rs267607504
hgdp	rs267607504
ensembl	rs267607504
geneview	rs267607504
scholar	rs267607504
google	rs267607504
pharmgkb	rs267607504
gwascentral	rs267607504
openSNP	rs267607504
23andMe	rs267607504
SNPshot	rs267607504
SNPdbe	rs267607504
MSV3d	rs267607504
GWAS Ctlg	rs267607504

Max Magnitude

0

ClinVar
Risk	rs267607504(C;C)
Alt	rs267607504(C;C)
Reference	Rs267607504(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.42992634A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056861.1, RCV000192102.1,