rs763868966

Orientation

plus

Stabilized

plus

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

Make rs763868966(A;A)

Make rs763868966(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44911429

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs763868966
dbSNP (classic)	rs763868966
ClinGen	rs763868966
ebi	rs763868966
HLI	rs763868966
Exac	rs763868966
Gnomad	rs763868966
Varsome	rs763868966
LitVar	rs763868966
Map	rs763868966
PheGenI	rs763868966
Biobank	rs763868966
1000 genomes	rs763868966
hgdp	rs763868966
ensembl	rs763868966
geneview	rs763868966
scholar	rs763868966
google	rs763868966
pharmgkb	rs763868966
gwascentral	rs763868966
openSNP	rs763868966
23andMe	rs763868966
SNPshot	rs763868966
SNPdbe	rs763868966
MSV3d	rs763868966
GWAS Ctlg	rs763868966

Max Magnitude

0

ClinVar
Risk	rs763868966(A;A) rs763868966(T;T)
Alt	rs763868966(A;A) rs763868966(T;T)
Reference	Rs763868966(C;C)
Significance	Other
Disease	Alexander's disease
Variation	info
Gene	GFAP
CLNDBN	Alexander's disease
Reversed	0
HGVS	NC_000017.10:g.42988797C>A
CLNSRC
CLNACC	RCV000192151.1,