rs58536923

Orientation

minus

Stabilized

minus

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

Make rs58536923(A;G)

Make rs58536923(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911743

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs58536923
dbSNP (classic)	rs58536923
ClinGen	rs58536923
ebi	rs58536923
HLI	rs58536923
Exac	rs58536923
Gnomad	rs58536923
Varsome	rs58536923
LitVar	rs58536923
Map	rs58536923
PheGenI	rs58536923
Biobank	rs58536923
1000 genomes	rs58536923
hgdp	rs58536923
ensembl	rs58536923
geneview	rs58536923
scholar	rs58536923
google	rs58536923
pharmgkb	rs58536923
gwascentral	rs58536923
openSNP	rs58536923
23andMe	rs58536923
SNPshot	rs58536923
SNPdbe	rs58536923
MSV3d	rs58536923
GWAS Ctlg	rs58536923

Max Magnitude

0

ClinVar
Risk	rs58536923(G;G)
Alt	rs58536923(G;G)
Reference	Rs58536923(A;A)
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.42989111T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056911.1, RCV000192149.1,