rs61497286

Orientation

minus

Stabilized

minus

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

Make rs61497286(C;T)

Make rs61497286(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44913318

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs61497286
dbSNP (classic)	rs61497286
ClinGen	rs61497286
ebi	rs61497286
HLI	rs61497286
Exac	rs61497286
Gnomad	rs61497286
Varsome	rs61497286
LitVar	rs61497286
Map	rs61497286
PheGenI	rs61497286
Biobank	rs61497286
1000 genomes	rs61497286
hgdp	rs61497286
ensembl	rs61497286
geneview	rs61497286
scholar	rs61497286
google	rs61497286
pharmgkb	rs61497286
gwascentral	rs61497286
openSNP	rs61497286
23andMe	rs61497286
SNPshot	rs61497286
SNPdbe	rs61497286
MSV3d	rs61497286
GWAS Ctlg	rs61497286

Max Magnitude

0

ClinVar
Risk	rs61497286(T;T)
Alt	rs61497286(T;T)
Reference	Rs61497286(C;C)
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.42990686G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056903.1, RCV000192139.1,