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rs2124349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2124349(A;A)
Make rs2124349(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position67349863
is asnp
is mentioned by
dbSNPrs2124349
ebirs2124349
HLIrs2124349
Exacrs2124349
Varsomers2124349
Maprs2124349
PheGenIrs2124349
hapmaprs2124349
1000 genomesrs2124349
hgdprs2124349
ensemblrs2124349
gopubmedrs2124349
geneviewrs2124349
scholarrs2124349
googlers2124349
pharmgkbrs2124349
gwascentralrs2124349
openSNPrs2124349
23andMers2124349
23andMe allrs2124349
SNP Nexus

SNPshotrs2124349
SNPdbers2124349
MSV3drs2124349
GWAS Ctlgrs2124349
GMAF0.05601
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 0.000004
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
rs2124349
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0546875
summary