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rs2160519

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs2160519(A;G)
Make rs2160519(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position13634912
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs2160519
ebirs2160519
HLIrs2160519
Exacrs2160519
Varsomers2160519
Maprs2160519
PheGenIrs2160519
hapmaprs2160519
1000 genomesrs2160519
hgdprs2160519
ensemblrs2160519
gopubmedrs2160519
geneviewrs2160519
scholarrs2160519
googlers2160519
pharmgkbrs2160519
gwascentralrs2160519
openSNPrs2160519
23andMers2160519
23andMe allrs2160519
SNP Nexus

SNPshotrs2160519
SNPdbers2160519
MSV3drs2160519
GWAS Ctlgrs2160519
GMAF0.06841
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 0.000002
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
rs2160519
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary