rs267607508

Orientation

minus

Stabilized

minus

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

Make rs267607508(A;A)

Make rs267607508(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44908128

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607508
dbSNP (classic)	rs267607508
ClinGen	rs267607508
ebi	rs267607508
HLI	rs267607508
Exac	rs267607508
Gnomad	rs267607508
Varsome	rs267607508
LitVar	rs267607508
Map	rs267607508
PheGenI	rs267607508
Biobank	rs267607508
1000 genomes	rs267607508
hgdp	rs267607508
ensembl	rs267607508
geneview	rs267607508
scholar	rs267607508
google	rs267607508
pharmgkb	rs267607508
gwascentral	rs267607508
openSNP	rs267607508
23andMe	rs267607508
SNPshot	rs267607508
SNPdbe	rs267607508
MSV3d	rs267607508
GWAS Ctlg	rs267607508

Max Magnitude

0

ClinVar
Risk	rs267607508(A;A) rs267607508(T;T)
Alt	rs267607508(A;A) rs267607508(T;T)
Reference	Rs267607508(C;C)
Significance	Pathogenic
Disease	Alexander's disease not provided
Variation	info
Gene	GFAP
CLNDBN	Alexander's disease not provided
Reversed	1
HGVS	NC_000017.10:g.42985496G>A; NC_000017.10:g.42985496G>T
CLNSRC
CLNACC	RCV000192183.1, RCV000056847.1, RCV000192184.1,