Have questions? Visit https://www.reddit.com/r/SNPedia

rs10810865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs10810865(C;C)
Make rs10810865(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position17895107
is asnp
is mentioned by
dbSNPrs10810865
ebirs10810865
HLIrs10810865
Exacrs10810865
Varsomers10810865
Maprs10810865
PheGenIrs10810865
hapmaprs10810865
1000 genomesrs10810865
hgdprs10810865
ensemblrs10810865
gopubmedrs10810865
geneviewrs10810865
scholarrs10810865
googlers10810865
pharmgkbrs10810865
gwascentralrs10810865
openSNPrs10810865
23andMers10810865
23andMe allrs10810865
SNP Nexus

SNPshotrs10810865
SNPdbers10810865
MSV3drs10810865
GWAS Ctlgrs10810865
GMAF0.08953
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 0.000004
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 4 x 10^-6) for paired associates learning (PAL) total errors at 6 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery


GET Evidence
rs10810865
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
summary