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rs10481151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1
Make rs10481151(C;T)
Make rs10481151(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position123819594
is asnp
is mentioned by
dbSNPrs10481151
ebirs10481151
HLIrs10481151
Exacrs10481151
Varsomers10481151
Maprs10481151
PheGenIrs10481151
hapmaprs10481151
1000 genomesrs10481151
hgdprs10481151
ensemblrs10481151
gopubmedrs10481151
geneviewrs10481151
scholarrs10481151
googlers10481151
pharmgkbrs10481151
gwascentralrs10481151
openSNPrs10481151
23andMers10481151
23andMe allrs10481151
SNP Nexus

SNPshotrs10481151
SNPdbers10481151
MSV3drs10481151
GWAS Ctlgrs10481151
GMAF0.2796
Max Magnitude1
? (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 4E-7
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 4 x 10^-7) for pattern recognition memory (PRM) percent correct in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs10481151
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.273438
summary