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rs61497286

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61497286(C;T)
Make rs61497286(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44913318
GeneGFAP
is asnp
is mentioned by
dbSNPrs61497286
ebirs61497286
HLIrs61497286
Exacrs61497286
Varsomers61497286
Maprs61497286
PheGenIrs61497286
hapmaprs61497286
1000 genomesrs61497286
hgdprs61497286
ensemblrs61497286
gopubmedrs61497286
geneviewrs61497286
scholarrs61497286
googlers61497286
pharmgkbrs61497286
gwascentralrs61497286
openSNPrs61497286
23andMers61497286
23andMe allrs61497286
SNP Nexus

SNPshotrs61497286
SNPdbers61497286
MSV3drs61497286
GWAS Ctlgrs61497286
Max Magnitude0
ClinVar
Risk rs61497286(T;T)
Alt rs61497286(T;T)
Reference rs61497286(C;C)
Significance Pathogenic
Disease not provided Alexander's disease
Variation info
Gene GFAP
CLNDBN not provided Alexander's disease
Reversed 1
HGVS NC_000017.10:g.42990686G>A
CLNSRC
CLNACC RCV000056903.1, RCV000192139.1,