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rs797044583

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044583(C;G)
Make rs797044583(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911710
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044583
ebirs797044583
HLIrs797044583
Exacrs797044583
Varsomers797044583
Maprs797044583
PheGenIrs797044583
hapmaprs797044583
1000 genomesrs797044583
hgdprs797044583
ensemblrs797044583
gopubmedrs797044583
geneviewrs797044583
scholarrs797044583
googlers797044583
pharmgkbrs797044583
gwascentralrs797044583
openSNPrs797044583
23andMers797044583
23andMe allrs797044583
SNP Nexus

SNPshotrs797044583
SNPdbers797044583
MSV3drs797044583
GWAS Ctlgrs797044583
Max Magnitude0
ClinVar
Risk rs797044583(G;G)
Alt rs797044583(G;G)
Reference rs797044583(C;C)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42989078G>C
CLNSRC
CLNACC RCV000192150.1,