rs267607500

Orientation

minus

Stabilized

minus

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

Make rs267607500(A;A)

Make rs267607500(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44913430

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs267607500
dbSNP (classic)	rs267607500
ClinGen	rs267607500
ebi	rs267607500
HLI	rs267607500
Exac	rs267607500
Gnomad	rs267607500
Varsome	rs267607500
LitVar	rs267607500
Map	rs267607500
PheGenI	rs267607500
Biobank	rs267607500
1000 genomes	rs267607500
hgdp	rs267607500
ensembl	rs267607500
geneview	rs267607500
scholar	rs267607500
google	rs267607500
pharmgkb	rs267607500
gwascentral	rs267607500
openSNP	rs267607500
23andMe	rs267607500
SNPshot	rs267607500
SNPdbe	rs267607500
MSV3d	rs267607500
GWAS Ctlg	rs267607500

Max Magnitude

0

ClinVar
Risk	rs267607500(A;A) rs267607500(C;C)
Alt	rs267607500(A;A) rs267607500(C;C)
Reference	Rs267607500(G;G)
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.42990798C>G; NC_000017.10:g.42990798C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056893.1, RCV000192129.1, RCV000056892.1, RCV000192128.1,