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rs797044572

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044572(C;C)
Make rs797044572(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915248
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044572
ebirs797044572
HLIrs797044572
Exacrs797044572
Varsomers797044572
Maprs797044572
PheGenIrs797044572
hapmaprs797044572
1000 genomesrs797044572
hgdprs797044572
ensemblrs797044572
gopubmedrs797044572
geneviewrs797044572
scholarrs797044572
googlers797044572
pharmgkbrs797044572
gwascentralrs797044572
openSNPrs797044572
23andMers797044572
23andMe allrs797044572
SNP Nexus

SNPshotrs797044572
SNPdbers797044572
MSV3drs797044572
GWAS Ctlgrs797044572
Max Magnitude0
ClinVar
Risk rs797044572(C;C)
Alt rs797044572(C;C)
Reference rs797044572(T;T)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42992616A>G
CLNSRC
CLNACC RCV000192113.1,