rs797044586

Orientation

minus

Stabilized

minus

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

Make rs797044586(C;T)

Make rs797044586(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911290

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs797044586
dbSNP (classic)	rs797044586
ClinGen	rs797044586
ebi	rs797044586
HLI	rs797044586
Exac	rs797044586
Gnomad	rs797044586
Varsome	rs797044586
LitVar	rs797044586
Map	rs797044586
PheGenI	rs797044586
Biobank	rs797044586
1000 genomes	rs797044586
hgdp	rs797044586
ensembl	rs797044586
geneview	rs797044586
scholar	rs797044586
google	rs797044586
pharmgkb	rs797044586
gwascentral	rs797044586
openSNP	rs797044586
23andMe	rs797044586
SNPshot	rs797044586
SNPdbe	rs797044586
MSV3d	rs797044586
GWAS Ctlg	rs797044586

Max Magnitude

0

ClinVar
Risk	rs797044586(T;T)
Alt	rs797044586(T;T)
Reference	Rs797044586(C;C)
Significance	Pathogenic
Disease	Alexander's disease
Variation	info
Gene	GFAP
CLNDBN	Alexander's disease
Reversed	1
HGVS	NC_000017.10:g.42988658G>A
CLNSRC
CLNACC	RCV000192158.1,