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

rs17001239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs17001239(C;T)
Make rs17001239(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position25630065
is asnp
is mentioned by
dbSNPrs17001239
ebirs17001239
HLIrs17001239
Exacrs17001239
Varsomers17001239
Maprs17001239
PheGenIrs17001239
hapmaprs17001239
1000 genomesrs17001239
hgdprs17001239
ensemblrs17001239
gopubmedrs17001239
geneviewrs17001239
scholarrs17001239
googlers17001239
pharmgkbrs17001239
gwascentralrs17001239
openSNPrs17001239
23andMers17001239
23andMe allrs17001239
SNP Nexus

SNPshotrs17001239
SNPdbers17001239
MSV3drs17001239
GWAS Ctlgrs17001239
GMAF0.1019
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 0.000002
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 2 x 10^-6) for pattern recognition memory (PRM) percent correct in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs17001239
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary