rs797044588

Orientation

minus

Stabilized

minus

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

Make rs797044588(A;G)

Make rs797044588(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911278

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs797044588
dbSNP (classic)	rs797044588
ClinGen	rs797044588
ebi	rs797044588
HLI	rs797044588
Exac	rs797044588
Gnomad	rs797044588
Varsome	rs797044588
LitVar	rs797044588
Map	rs797044588
PheGenI	rs797044588
Biobank	rs797044588
1000 genomes	rs797044588
hgdp	rs797044588
ensembl	rs797044588
geneview	rs797044588
scholar	rs797044588
google	rs797044588
pharmgkb	rs797044588
gwascentral	rs797044588
openSNP	rs797044588
23andMe	rs797044588
SNPshot	rs797044588
SNPdbe	rs797044588
MSV3d	rs797044588
GWAS Ctlg	rs797044588

Max Magnitude

0

ClinVar
Risk	rs797044588(G;G)
Alt	rs797044588(G;G)
Reference	Rs797044588(A;A)
Significance	Pathogenic
Disease	Alexander's disease
Variation	info
Gene	GFAP
CLNDBN	Alexander's disease
Reversed	1
HGVS	NC_000017.10:g.42988646T>C
CLNSRC
CLNACC	RCV000192163.1,