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rs767210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs767210(C;T)
Make rs767210(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position110817691
GeneLOC100129390
is asnp
is mentioned by
dbSNPrs767210
ebirs767210
HLIrs767210
Exacrs767210
Varsomers767210
Maprs767210
PheGenIrs767210
hapmaprs767210
1000 genomesrs767210
hgdprs767210
ensemblrs767210
gopubmedrs767210
geneviewrs767210
scholarrs767210
googlers767210
pharmgkbrs767210
gwascentralrs767210
openSNPrs767210
23andMers767210
23andMe allrs767210
SNP Nexus

SNPshotrs767210
SNPdbers767210
MSV3drs767210
GWAS Ctlgrs767210
GMAF0.06979
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 3E-7
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 3 x 10^-7) for paired associates learning (PAL) total errors at 6 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery


GET Evidence
rs767210
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0703125
summary