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rs797044589

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044589(A;C)
Make rs797044589(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911245
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044589
ebirs797044589
HLIrs797044589
Exacrs797044589
Varsomers797044589
Maprs797044589
PheGenIrs797044589
hapmaprs797044589
1000 genomesrs797044589
hgdprs797044589
ensemblrs797044589
gopubmedrs797044589
geneviewrs797044589
scholarrs797044589
googlers797044589
pharmgkbrs797044589
gwascentralrs797044589
openSNPrs797044589
23andMers797044589
23andMe allrs797044589
SNP Nexus

SNPshotrs797044589
SNPdbers797044589
MSV3drs797044589
GWAS Ctlgrs797044589
Max Magnitude0
ClinVar
Risk rs797044589(C;C)
Alt rs797044589(C;C)
Reference rs797044589(A;A)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42988613T>G
CLNSRC
CLNACC RCV000192175.1,