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rs7729273

From SNPedia

Orientationplus
Stabilizedplus
Make rs7729273(C;C)
Make rs7729273(C;T)
Make rs7729273(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position7227934
is asnp
is mentioned by
dbSNPrs7729273
ebirs7729273
HLIrs7729273
Exacrs7729273
Varsomers7729273
Maprs7729273
PheGenIrs7729273
hapmaprs7729273
1000 genomesrs7729273
hgdprs7729273
ensemblrs7729273
gopubmedrs7729273
geneviewrs7729273
scholarrs7729273
googlers7729273
pharmgkbrs7729273
gwascentralrs7729273
openSNPrs7729273
23andMers7729273
23andMe allrs7729273
SNP Nexus

SNPshotrs7729273
SNPdbers7729273
MSV3drs7729273
GWAS Ctlgrs7729273
GMAF0.1607
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 0.000001
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, top hit for spatial span (SSP) length in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs7729273
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary