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rs797044588

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044588(A;G)
Make rs797044588(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911278
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044588
ebirs797044588
HLIrs797044588
Exacrs797044588
Varsomers797044588
Maprs797044588
PheGenIrs797044588
hapmaprs797044588
1000 genomesrs797044588
hgdprs797044588
ensemblrs797044588
gopubmedrs797044588
geneviewrs797044588
scholarrs797044588
googlers797044588
pharmgkbrs797044588
gwascentralrs797044588
openSNPrs797044588
23andMers797044588
23andMe allrs797044588
SNP Nexus

SNPshotrs797044588
SNPdbers797044588
MSV3drs797044588
GWAS Ctlgrs797044588
Max Magnitude0
ClinVar
Risk rs797044588(G;G)
Alt rs797044588(G;G)
Reference rs797044588(A;A)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42988646T>C
CLNSRC
CLNACC RCV000192163.1,