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rs267607504

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607504(C;C)
Make rs267607504(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915266
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607504
ebirs267607504
HLIrs267607504
Exacrs267607504
Varsomers267607504
Maprs267607504
PheGenIrs267607504
hapmaprs267607504
1000 genomesrs267607504
hgdprs267607504
ensemblrs267607504
gopubmedrs267607504
geneviewrs267607504
scholarrs267607504
googlers267607504
pharmgkbrs267607504
gwascentralrs267607504
openSNPrs267607504
23andMers267607504
23andMe allrs267607504
SNP Nexus

SNPshotrs267607504
SNPdbers267607504
MSV3drs267607504
GWAS Ctlgrs267607504
Max Magnitude0
ClinVar
Risk rs267607504(C;C)
Alt rs267607504(C;C)
Reference rs267607504(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.42992634A>G
CLNSRC
CLNACC RCV000056861.1, RCV000192102.1,