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rs816488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs816488(C;C)
Make rs816488(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position39512297
GeneMOBP
is asnp
is mentioned by
dbSNPrs816488
ebirs816488
HLIrs816488
Exacrs816488
Varsomers816488
Maprs816488
PheGenIrs816488
hapmaprs816488
1000 genomesrs816488
hgdprs816488
ensemblrs816488
gopubmedrs816488
geneviewrs816488
scholarrs816488
googlers816488
pharmgkbrs816488
gwascentralrs816488
openSNPrs816488
23andMers816488
23andMe allrs816488
SNP Nexus

SNPshotrs816488
SNPdbers816488
MSV3drs816488
GWAS Ctlgrs816488
GMAF0.07668
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.000004
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 4 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs816488
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.882812
summary