rs267607509

Orientation

minus

Stabilized

minus

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

Make rs267607509(A;A)

Make rs267607509(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44915105

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607509
dbSNP (classic)	rs267607509
ClinGen	rs267607509
ebi	rs267607509
HLI	rs267607509
Exac	rs267607509
Gnomad	rs267607509
Varsome	rs267607509
LitVar	rs267607509
Map	rs267607509
PheGenI	rs267607509
Biobank	rs267607509
1000 genomes	rs267607509
hgdp	rs267607509
ensembl	rs267607509
geneview	rs267607509
scholar	rs267607509
google	rs267607509
pharmgkb	rs267607509
gwascentral	rs267607509
openSNP	rs267607509
23andMe	rs267607509
SNPshot	rs267607509
SNPdbe	rs267607509
MSV3d	rs267607509
GWAS Ctlg	rs267607509

Max Magnitude

0

ClinVar
Risk	rs267607509(A;A)
Alt	rs267607509(A;A)
Reference	Rs267607509(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.42992473C>T
CLNSRC
CLNACC	RCV000056885.1, RCV000192126.1,