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

rs267607507

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607507(A;A)
Make rs267607507(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44913733
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607507
ebirs267607507
HLIrs267607507
Exacrs267607507
Varsomers267607507
Maprs267607507
PheGenIrs267607507
hapmaprs267607507
1000 genomesrs267607507
hgdprs267607507
ensemblrs267607507
gopubmedrs267607507
geneviewrs267607507
scholarrs267607507
googlers267607507
pharmgkbrs267607507
gwascentralrs267607507
openSNPrs267607507
23andMers267607507
23andMe allrs267607507
SNP Nexus

SNPshotrs267607507
SNPdbers267607507
MSV3drs267607507
GWAS Ctlgrs267607507
Max Magnitude0
ClinVar
Risk rs267607507(A;A)
Alt rs267607507(A;A)
Reference rs267607507(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.42991101C>T
CLNSRC
CLNACC RCV000056889.1, RCV000192127.1,