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rs267607515

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607515(C;C)
Make rs267607515(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911293
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607515
ebirs267607515
HLIrs267607515
Exacrs267607515
Varsomers267607515
Maprs267607515
PheGenIrs267607515
hapmaprs267607515
1000 genomesrs267607515
hgdprs267607515
ensemblrs267607515
gopubmedrs267607515
geneviewrs267607515
scholarrs267607515
googlers267607515
pharmgkbrs267607515
gwascentralrs267607515
openSNPrs267607515
23andMers267607515
23andMe allrs267607515
SNP Nexus

SNPshotrs267607515
SNPdbers267607515
MSV3drs267607515
GWAS Ctlgrs267607515
Max Magnitude0
ClinVar
Risk rs267607515(A,C;A,C)
Alt rs267607515(A,C;A,C)
Reference rs267607515(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.42988661A>G
CLNSRC
CLNACC RCV000056821.1, RCV000192157.1,