Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607509

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607509(A;A)
Make rs267607509(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915105
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607509
ebirs267607509
HLIrs267607509
Exacrs267607509
Varsomers267607509
Maprs267607509
PheGenIrs267607509
hapmaprs267607509
1000 genomesrs267607509
hgdprs267607509
ensemblrs267607509
gopubmedrs267607509
geneviewrs267607509
scholarrs267607509
googlers267607509
pharmgkbrs267607509
gwascentralrs267607509
openSNPrs267607509
23andMers267607509
23andMe allrs267607509
SNP Nexus

SNPshotrs267607509
SNPdbers267607509
MSV3drs267607509
GWAS Ctlgrs267607509
Max Magnitude0
ClinVar
Risk rs267607509(A;A)
Alt rs267607509(A;A)
Reference rs267607509(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.42992473C>T
CLNSRC
CLNACC RCV000056885.1, RCV000192126.1,