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rs797044586

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044586(C;T)
Make rs797044586(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911290
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044586
ebirs797044586
HLIrs797044586
Exacrs797044586
Varsomers797044586
Maprs797044586
PheGenIrs797044586
hapmaprs797044586
1000 genomesrs797044586
hgdprs797044586
ensemblrs797044586
gopubmedrs797044586
geneviewrs797044586
scholarrs797044586
googlers797044586
pharmgkbrs797044586
gwascentralrs797044586
openSNPrs797044586
23andMers797044586
23andMe allrs797044586
SNP Nexus

SNPshotrs797044586
SNPdbers797044586
MSV3drs797044586
GWAS Ctlgrs797044586
Max Magnitude0
ClinVar
Risk rs797044586(T;T)
Alt rs797044586(T;T)
Reference rs797044586(C;C)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42988658G>A
CLNSRC
CLNACC RCV000192158.1,