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rs797044574

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044574(A;C)
Make rs797044574(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44915209
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044574
ebirs797044574
HLIrs797044574
Exacrs797044574
Varsomers797044574
Maprs797044574
PheGenIrs797044574
hapmaprs797044574
1000 genomesrs797044574
hgdprs797044574
ensemblrs797044574
gopubmedrs797044574
geneviewrs797044574
scholarrs797044574
googlers797044574
pharmgkbrs797044574
gwascentralrs797044574
openSNPrs797044574
23andMers797044574
23andMe allrs797044574
SNP Nexus

SNPshotrs797044574
SNPdbers797044574
MSV3drs797044574
GWAS Ctlgrs797044574
Max Magnitude0
ClinVar
Risk rs797044574(C;C)
Alt rs797044574(C;C)
Reference rs797044574(A;A)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42992577T>G
CLNSRC
CLNACC RCV000192121.1,