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rs60825166

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs60825166(C;G)
Make rs60825166(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44911288
GeneGFAP
is asnp
is mentioned by
dbSNPrs60825166
ebirs60825166
HLIrs60825166
Exacrs60825166
Varsomers60825166
Maprs60825166
PheGenIrs60825166
hapmaprs60825166
1000 genomesrs60825166
hgdprs60825166
ensemblrs60825166
gopubmedrs60825166
geneviewrs60825166
scholarrs60825166
googlers60825166
pharmgkbrs60825166
gwascentralrs60825166
openSNPrs60825166
23andMers60825166
23andMe allrs60825166
SNP Nexus

SNPshotrs60825166
SNPdbers60825166
MSV3drs60825166
GWAS Ctlgrs60825166
Max Magnitude0
ClinVar
Risk rs60825166(G;G)
Alt rs60825166(G;G)
Reference rs60825166(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.42988656G>C
CLNSRC
CLNACC RCV000056822.1, RCV000192160.1,