rs267607518

Orientation

minus

Stabilized

minus

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

Make rs267607518(C;C)

Make rs267607518(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44915228

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607518
dbSNP (classic)	rs267607518
ClinGen	rs267607518
ebi	rs267607518
HLI	rs267607518
Exac	rs267607518
Gnomad	rs267607518
Varsome	rs267607518
LitVar	rs267607518
Map	rs267607518
PheGenI	rs267607518
Biobank	rs267607518
1000 genomes	rs267607518
hgdp	rs267607518
ensembl	rs267607518
geneview	rs267607518
scholar	rs267607518
google	rs267607518
pharmgkb	rs267607518
gwascentral	rs267607518
openSNP	rs267607518
23andMe	rs267607518
SNPshot	rs267607518
SNPdbe	rs267607518
MSV3d	rs267607518
GWAS Ctlg	rs267607518

Max Magnitude

0

ClinVar
Risk	rs267607518(A;A) rs267607518(C;C) rs267607518(T;T)
Alt	rs267607518(A;A) rs267607518(C;C) rs267607518(T;T)
Reference	Rs267607518(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.42992596C>G; NC_000017.10:g.42992596C>T
CLNSRC
CLNACC	RCV000056876.1, RCV000192118.1, RCV000192117.1,