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rs16832015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16832015(C;T)
Make rs16832015(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160452126
is asnp
is mentioned by
dbSNPrs16832015
ebirs16832015
HLIrs16832015
Exacrs16832015
Varsomers16832015
Maprs16832015
PheGenIrs16832015
hapmaprs16832015
1000 genomesrs16832015
hgdprs16832015
ensemblrs16832015
gopubmedrs16832015
geneviewrs16832015
scholarrs16832015
googlers16832015
pharmgkbrs16832015
gwascentralrs16832015
openSNPrs16832015
23andMers16832015
23andMe allrs16832015
SNP Nexus

SNPshotrs16832015
SNPdbers16832015
MSV3drs16832015
GWAS Ctlgrs16832015
GMAF0.02571
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 0.000002
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 2 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs16832015
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0078125
summary