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rs267607511

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607511(C;C)
Make rs267607511(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911287
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607511
ebirs267607511
HLIrs267607511
Exacrs267607511
Varsomers267607511
Maprs267607511
PheGenIrs267607511
hapmaprs267607511
1000 genomesrs267607511
hgdprs267607511
ensemblrs267607511
gopubmedrs267607511
geneviewrs267607511
scholarrs267607511
googlers267607511
pharmgkbrs267607511
gwascentralrs267607511
openSNPrs267607511
23andMers267607511
23andMe allrs267607511
SNP Nexus

SNPshotrs267607511
SNPdbers267607511
MSV3drs267607511
GWAS Ctlgrs267607511
Max Magnitude0
ClinVar
Risk rs267607511(C;C)
Alt rs267607511(C;C)
Reference rs267607511(T;T)
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.42988655A>G
CLNSRC
CLNACC RCV000056823.1, RCV000192161.1,