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rs797044571

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044571(A;A)
Make rs797044571(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915255
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044571
ebirs797044571
HLIrs797044571
Exacrs797044571
Varsomers797044571
Maprs797044571
PheGenIrs797044571
hapmaprs797044571
1000 genomesrs797044571
hgdprs797044571
ensemblrs797044571
gopubmedrs797044571
geneviewrs797044571
scholarrs797044571
googlers797044571
pharmgkbrs797044571
gwascentralrs797044571
openSNPrs797044571
23andMers797044571
23andMe allrs797044571
SNP Nexus

SNPshotrs797044571
SNPdbers797044571
MSV3drs797044571
GWAS Ctlgrs797044571
Max Magnitude0
ClinVar
Risk rs797044571(A;A)
Alt rs797044571(A;A)
Reference rs797044571(G;G)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42992623C>T
CLNSRC
CLNACC RCV000192108.1,