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rs797044585

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044585(C;C)
Make rs797044585(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911312
GeneGFAP
is asnp
is mentioned by
dbSNPrs797044585
ebirs797044585
HLIrs797044585
Exacrs797044585
Varsomers797044585
Maprs797044585
PheGenIrs797044585
hapmaprs797044585
1000 genomesrs797044585
hgdprs797044585
ensemblrs797044585
gopubmedrs797044585
geneviewrs797044585
scholarrs797044585
googlers797044585
pharmgkbrs797044585
gwascentralrs797044585
openSNPrs797044585
23andMers797044585
23andMe allrs797044585
SNP Nexus

SNPshotrs797044585
SNPdbers797044585
MSV3drs797044585
GWAS Ctlgrs797044585
Max Magnitude0
ClinVar
Risk rs797044585(C;C)
Alt rs797044585(C;C)
Reference rs797044585(G;G)
Significance Pathogenic
Disease Alexander's disease
Variation info
Gene GFAP
CLNDBN Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42988680C>G
CLNSRC
CLNACC RCV000192156.1,