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rs6592284

From SNPedia

Orientationplus
Stabilizedplus
Make rs6592284(C;C)
Make rs6592284(C;T)
Make rs6592284(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position86344859
GeneC11orf73
is asnp
is mentioned by
dbSNPrs6592284
ebirs6592284
HLIrs6592284
Exacrs6592284
Varsomers6592284
Maprs6592284
PheGenIrs6592284
hapmaprs6592284
1000 genomesrs6592284
hgdprs6592284
ensemblrs6592284
gopubmedrs6592284
geneviewrs6592284
scholarrs6592284
googlers6592284
pharmgkbrs6592284
gwascentralrs6592284
openSNPrs6592284
23andMers6592284
23andMe allrs6592284
SNP Nexus

SNPshotrs6592284
SNPdbers6592284
MSV3drs6592284
GWAS Ctlgrs6592284
GMAF0.2828
Max Magnitude
? (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, top hit for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery), noted as close to ME3 which has shown expression changes in a rat model of schizophrenia ( [PMID 10485705] )


GET Evidence
rs6592284
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.261905
summary