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rs9300212

From SNPedia

Orientationplus
Stabilizedplus
Make rs9300212(C;C)
Make rs9300212(C;T)
Make rs9300212(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position33548231
is asnp
is mentioned by
dbSNPrs9300212
ebirs9300212
HLIrs9300212
Exacrs9300212
Varsomers9300212
Maprs9300212
PheGenIrs9300212
hapmaprs9300212
1000 genomesrs9300212
hgdprs9300212
ensemblrs9300212
gopubmedrs9300212
geneviewrs9300212
scholarrs9300212
googlers9300212
pharmgkbrs9300212
gwascentralrs9300212
openSNPrs9300212
23andMers9300212
23andMe allrs9300212
SNP Nexus

SNPshotrs9300212
SNPdbers9300212
MSV3drs9300212
GWAS Ctlgrs9300212
GMAF0.4118
Max Magnitude
? (C;C) (C;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 0.0000079999999999999996
Odds Ratio NR NR

[PMID 17903297OA-icon.png] non sig. gwas, top 25 GEE p-values, Wide-Range Achievement Test


[PMID 21304891OA-icon.png] A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.


GET Evidence
rs9300212
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5625
summary