Have questions? Visit https://www.reddit.com/r/SNPedia

rs530965

From SNPedia

Orientationminus
Stabilizedminus
Make rs530965(A;A)
Make rs530965(A;G)
Make rs530965(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position79354056
GeneTENM4
is asnp
is mentioned by
dbSNPrs530965
ebirs530965
HLIrs530965
Exacrs530965
Varsomers530965
Maprs530965
PheGenIrs530965
hapmaprs530965
1000 genomesrs530965
hgdprs530965
ensemblrs530965
gopubmedrs530965
geneviewrs530965
scholarrs530965
googlers530965
pharmgkbrs530965
gwascentralrs530965
openSNPrs530965
23andMers530965
23andMe allrs530965
SNP Nexus

SNPshotrs530965
SNPdbers530965
MSV3drs530965
GWAS Ctlgrs530965
GMAF0.4949
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.0000039999999999999998
Odds Ratio NR NR

[PMID 17903297OA-icon.png] non sig. gwas, top 25 GEE p-values, Boston Naming Test


GET Evidence
rs530965
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.429688
summary