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rs797044577

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044577(A;A)
Make rs797044577(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44913357
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044577
ebirs797044577
HLIrs797044577
Exacrs797044577
Varsomers797044577
Maprs797044577
PheGenIrs797044577
hapmaprs797044577
1000 genomesrs797044577
hgdprs797044577
ensemblrs797044577
gopubmedrs797044577
geneviewrs797044577
scholarrs797044577
googlers797044577
pharmgkbrs797044577
gwascentralrs797044577
openSNPrs797044577
23andMers797044577
23andMe allrs797044577
SNP Nexus

SNPshotrs797044577
SNPdbers797044577
MSV3drs797044577
GWAS Ctlgrs797044577
Max Magnitude0
ClinVar
Risk rs797044577(A;A)
Alt rs797044577(A;A)
Reference rs797044577(T;T)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42990725A>T
CLNSRC
CLNACC RCV000192132.1,