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rs61726471

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61726471(A;T)
Make rs61726471(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44910629
GeneGFAP
is asnp
is mentioned by
dbSNPrs61726471
ebirs61726471
HLIrs61726471
Exacrs61726471
Varsomers61726471
Maprs61726471
PheGenIrs61726471
hapmaprs61726471
1000 genomesrs61726471
hgdprs61726471
ensemblrs61726471
gopubmedrs61726471
geneviewrs61726471
scholarrs61726471
googlers61726471
pharmgkbrs61726471
gwascentralrs61726471
openSNPrs61726471
23andMers61726471
23andMe allrs61726471
SNP Nexus

SNPshotrs61726471
SNPdbers61726471
MSV3drs61726471
GWAS Ctlgrs61726471
Max Magnitude0
ClinVar
Risk rs61726471(T;T)
Alt rs61726471(T;T)
Reference rs61726471(A;A)
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.42987997T>A
CLNSRC
CLNACC RCV000056842.1, RCV000192181.1,