rs267607513

Orientation

minus

Stabilized

minus

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

Make rs267607513(C;G)

Make rs267607513(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911375

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607513
dbSNP (classic)	rs267607513
ClinGen	rs267607513
ebi	rs267607513
HLI	rs267607513
Exac	rs267607513
Gnomad	rs267607513
Varsome	rs267607513
LitVar	rs267607513
Map	rs267607513
PheGenI	rs267607513
Biobank	rs267607513
1000 genomes	rs267607513
hgdp	rs267607513
ensembl	rs267607513
geneview	rs267607513
scholar	rs267607513
google	rs267607513
pharmgkb	rs267607513
gwascentral	rs267607513
openSNP	rs267607513
23andMe	rs267607513
SNPshot	rs267607513
SNPdbe	rs267607513
MSV3d	rs267607513
GWAS Ctlg	rs267607513

Max Magnitude

0

ClinVar
Risk	rs267607513(G;G)
Alt	rs267607513(G;G)
Reference	Rs267607513(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.42988743G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056917.1, RCV000192152.1,