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rs267607502

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607502(A;G)
Make rs267607502(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911266
GeneGFAP
is asnp
is mentioned by
dbSNPrs267607502
ebirs267607502
HLIrs267607502
Exacrs267607502
Varsomers267607502
Maprs267607502
PheGenIrs267607502
hapmaprs267607502
1000 genomesrs267607502
hgdprs267607502
ensemblrs267607502
gopubmedrs267607502
geneviewrs267607502
scholarrs267607502
googlers267607502
pharmgkbrs267607502
gwascentralrs267607502
openSNPrs267607502
23andMers267607502
23andMe allrs267607502
SNP Nexus

SNPshotrs267607502
SNPdbers267607502
MSV3drs267607502
GWAS Ctlgrs267607502
Max Magnitude0
ClinVar
Risk rs267607502(G;G)
Alt rs267607502(G;G)
Reference rs267607502(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.42988634T>C
CLNSRC
CLNACC RCV000056829.1, RCV000192168.1,