rs267607512

Orientation

minus

Stabilized

minus

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

Make rs267607512(C;T)

Make rs267607512(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911237

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607512
dbSNP (classic)	rs267607512
ClinGen	rs267607512
ebi	rs267607512
HLI	rs267607512
Exac	rs267607512
Gnomad	rs267607512
Varsome	rs267607512
LitVar	rs267607512
Map	rs267607512
PheGenI	rs267607512
Biobank	rs267607512
1000 genomes	rs267607512
hgdp	rs267607512
ensembl	rs267607512
geneview	rs267607512
scholar	rs267607512
google	rs267607512
pharmgkb	rs267607512
gwascentral	rs267607512
openSNP	rs267607512
23andMe	rs267607512
SNPshot	rs267607512
SNPdbe	rs267607512
MSV3d	rs267607512
GWAS Ctlg	rs267607512

Max Magnitude

0

ClinVar
Risk	rs267607512(G;G) rs267607512(T;T)
Alt	rs267607512(G;G) rs267607512(T;T)
Reference	Rs267607512(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.42988605G>A; NC_000017.10:g.42988605G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056837.1, RCV000192177.1, RCV000056836.1,