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rs267607510

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607510(A;A)
Make rs267607510(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915278
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607510
ebirs267607510
HLIrs267607510
Exacrs267607510
Varsomers267607510
Maprs267607510
PheGenIrs267607510
hapmaprs267607510
1000 genomesrs267607510
hgdprs267607510
ensemblrs267607510
gopubmedrs267607510
geneviewrs267607510
scholarrs267607510
googlers267607510
pharmgkbrs267607510
gwascentralrs267607510
openSNPrs267607510
23andMers267607510
23andMe allrs267607510
SNP Nexus

SNPshotrs267607510
SNPdbers267607510
MSV3drs267607510
GWAS Ctlgrs267607510
Max Magnitude0
ClinVar
Risk rs267607510(A;A)
Alt rs267607510(A;A)
Reference rs267607510(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.42992646C>T
CLNSRC
CLNACC RCV000056856.1, RCV000192099.1,