rs121909718

Orientation

minus

Stabilized

minus

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

Make rs121909718(C;C)

Make rs121909718(C;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

44911277

Gene

GFAP

is a	snp
is	mentioned by
dbSNP	rs121909718
dbSNP (classic)	rs121909718
ClinGen	rs121909718
ebi	rs121909718
HLI	rs121909718
Exac	rs121909718
Gnomad	rs121909718
Varsome	rs121909718
LitVar	rs121909718
Map	rs121909718
PheGenI	rs121909718
Biobank	rs121909718
1000 genomes	rs121909718
hgdp	rs121909718
ensembl	rs121909718
geneview	rs121909718
scholar	rs121909718
google	rs121909718
pharmgkb	rs121909718
gwascentral	rs121909718
openSNP	rs121909718
23andMe	rs121909718
SNPshot	rs121909718
SNPdbe	rs121909718
MSV3d	rs121909718
GWAS Ctlg	rs121909718

Merged from

Rs28932768

Max Magnitude

0

OMIM	137780
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121909718(C;C)
Alt	rs121909718(C;C)
Reference	Rs121909718(G;G)
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.42988645C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017559.33, RCV000056825.1,