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rs2289681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2289681(C;T)
Make rs2289681(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position44911720
GeneGFAP
is asnp
is mentioned by
dbSNPrs2289681
ebirs2289681
HLIrs2289681
Exacrs2289681
Varsomers2289681
Maprs2289681
PheGenIrs2289681
hapmaprs2289681
1000 genomesrs2289681
hgdprs2289681
ensemblrs2289681
gopubmedrs2289681
geneviewrs2289681
scholarrs2289681
googlers2289681
pharmgkbrs2289681
gwascentralrs2289681
openSNPrs2289681
23andMers2289681
23andMe allrs2289681
SNP Nexus

SNPshotrs2289681
SNPdbers2289681
MSV3drs2289681
GWAS Ctlgrs2289681
GMAF0.1423
Max Magnitude0
? (C;C) (C;T) (T;T) 28
Mentioned in a 23andMe discussion on intelligence.

Synonymous Polymorphisms at Splicing Regulatory Sites are Associated with CpGs in Neurodegenerative Disease-Related Genes.[PMID 20077034]


ClinVar
Risk rs2289681(T;T)
Alt rs2289681(T;T)
Reference rs2289681(C;C)
Significance Untested
Disease not provided
Variation info
Gene GFAP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.42989088C>T
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000056912.1,