rs267607507

Orientation

minus

Stabilized

minus

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

Make rs267607507(A;A)

Make rs267607507(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44913733

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607507
dbSNP (classic)	rs267607507
ClinGen	rs267607507
ebi	rs267607507
HLI	rs267607507
Exac	rs267607507
Gnomad	rs267607507
Varsome	rs267607507
LitVar	rs267607507
Map	rs267607507
PheGenI	rs267607507
Biobank	rs267607507
1000 genomes	rs267607507
hgdp	rs267607507
ensembl	rs267607507
geneview	rs267607507
scholar	rs267607507
google	rs267607507
pharmgkb	rs267607507
gwascentral	rs267607507
openSNP	rs267607507
23andMe	rs267607507
SNPshot	rs267607507
SNPdbe	rs267607507
MSV3d	rs267607507
GWAS Ctlg	rs267607507

Max Magnitude

0

ClinVar
Risk	rs267607507(A;A)
Alt	rs267607507(A;A)
Reference	Rs267607507(G;G)
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.42991101C>T
CLNSRC
CLNACC	RCV000056889.1, RCV000192127.1,