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rs6799705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6799705(C;T)
Make rs6799705(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position35940638
is asnp
is mentioned by
dbSNPrs6799705
ebirs6799705
HLIrs6799705
Exacrs6799705
Varsomers6799705
Maprs6799705
PheGenIrs6799705
hapmaprs6799705
1000 genomesrs6799705
hgdprs6799705
ensemblrs6799705
gopubmedrs6799705
geneviewrs6799705
scholarrs6799705
googlers6799705
pharmgkbrs6799705
gwascentralrs6799705
openSNPrs6799705
23andMers6799705
23andMe allrs6799705
SNP Nexus

SNPshotrs6799705
SNPdbers6799705
MSV3drs6799705
GWAS Ctlgrs6799705
GMAF0.05969
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 2E-7
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 2 x 10^-7) for paired associates learning (PAL) total errors at 8 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery


GET Evidence
rs6799705
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary