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rs934299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs934299(G;T)
Make rs934299(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position136581370
is asnp
is mentioned by
dbSNPrs934299
ebirs934299
HLIrs934299
Exacrs934299
Varsomers934299
Maprs934299
PheGenIrs934299
hapmaprs934299
1000 genomesrs934299
hgdprs934299
ensemblrs934299
gopubmedrs934299
geneviewrs934299
scholarrs934299
googlers934299
pharmgkbrs934299
gwascentralrs934299
openSNPrs934299
23andMers934299
23andMe allrs934299
SNP Nexus

SNPshotrs934299
SNPdbers934299
MSV3drs934299
GWAS Ctlgrs934299
GMAF0.1276
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 17903297OA-icon.png]
Trait Cognitive test performance
Title Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study
Risk Allele
P-val 0.0000090000000000000002
Odds Ratio NR NR

[PMID 17903297OA-icon.png] non sig. gwas, top 25 GEE p-values, measure of attention and executive function


GET Evidence
rs934299
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary