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rs960089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs960089(A;A)
Make rs960089(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position58795750
is asnp
is mentioned by
dbSNPrs960089
ebirs960089
HLIrs960089
Exacrs960089
Varsomers960089
Maprs960089
PheGenIrs960089
hapmaprs960089
1000 genomesrs960089
hgdprs960089
ensemblrs960089
gopubmedrs960089
geneviewrs960089
scholarrs960089
googlers960089
pharmgkbrs960089
gwascentralrs960089
openSNPrs960089
23andMers960089
23andMe allrs960089
SNP Nexus

SNPshotrs960089
SNPdbers960089
MSV3drs960089
GWAS Ctlgrs960089
GMAF0.06979
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19734545OA-icon.png]
Trait Cognitive performance
Title A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery
Risk Allele
P-val 0.000006
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 6 x 10^-6) for paired associates learning (PAL) total errors at 6 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery


GET Evidence
rs960089
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary