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rs797044578

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044578(C;T)
Make rs797044578(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44913277
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044578
ebirs797044578
HLIrs797044578
Exacrs797044578
Varsomers797044578
Maprs797044578
PheGenIrs797044578
hapmaprs797044578
1000 genomesrs797044578
hgdprs797044578
ensemblrs797044578
gopubmedrs797044578
geneviewrs797044578
scholarrs797044578
googlers797044578
pharmgkbrs797044578
gwascentralrs797044578
openSNPrs797044578
23andMers797044578
23andMe allrs797044578
SNP Nexus

SNPshotrs797044578
SNPdbers797044578
MSV3drs797044578
GWAS Ctlgrs797044578
Max Magnitude0
ClinVar
Risk rs797044578(T;T)
Alt rs797044578(T;T)
Reference rs797044578(C;C)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42990645G>A
CLNSRC
CLNACC RCV000192143.1,