rs62636501

Orientation

minus

Stabilized

minus

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

Make rs62636501(A;T)

Make rs62636501(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911284

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs62636501
dbSNP (classic)	rs62636501
ClinGen	rs62636501
ebi	rs62636501
HLI	rs62636501
Exac	rs62636501
Gnomad	rs62636501
Varsome	rs62636501
LitVar	rs62636501
Map	rs62636501
PheGenI	rs62636501
Biobank	rs62636501
1000 genomes	rs62636501
hgdp	rs62636501
ensembl	rs62636501
geneview	rs62636501
scholar	rs62636501
google	rs62636501
pharmgkb	rs62636501
gwascentral	rs62636501
openSNP	rs62636501
23andMe	rs62636501
SNPshot	rs62636501
SNPdbe	rs62636501
MSV3d	rs62636501
GWAS Ctlg	rs62636501

Max Magnitude

0

ClinVar
Risk	rs62636501(T;T)
Alt	rs62636501(T;T)
Reference	Rs62636501(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.42988652T>A
CLNSRC
CLNACC	RCV000056824.1, RCV000192162.1,