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rs267607521

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607521(A;T)
Make rs267607521(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44907369
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607521
ebirs267607521
HLIrs267607521
Exacrs267607521
Varsomers267607521
Maprs267607521
PheGenIrs267607521
hapmaprs267607521
1000 genomesrs267607521
hgdprs267607521
ensemblrs267607521
gopubmedrs267607521
geneviewrs267607521
scholarrs267607521
googlers267607521
pharmgkbrs267607521
gwascentralrs267607521
openSNPrs267607521
23andMers267607521
23andMe allrs267607521
SNP Nexus

SNPshotrs267607521
SNPdbers267607521
MSV3drs267607521
GWAS Ctlgrs267607521
Max Magnitude0
ClinVar
Risk rs267607521(T;T)
Alt rs267607521(T;T)
Reference rs267607521(A;A)
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.42984737T>A
CLNSRC
CLNACC RCV000056851.1, RCV000192188.1,