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rs4601609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4601609(C;C)
Make rs4601609(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position58859954
GeneOR4X1
is asnp
is mentioned by
dbSNPrs4601609
ebirs4601609
HLIrs4601609
Exacrs4601609
Varsomers4601609
Maprs4601609
PheGenIrs4601609
hapmaprs4601609
1000 genomesrs4601609
hgdprs4601609
ensemblrs4601609
gopubmedrs4601609
geneviewrs4601609
scholarrs4601609
googlers4601609
pharmgkbrs4601609
gwascentralrs4601609
openSNPrs4601609
23andMers4601609
23andMe allrs4601609
SNP Nexus

SNPshotrs4601609
SNPdbers4601609
MSV3drs4601609
GWAS Ctlgrs4601609
GMAF0.08586
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 0.000005
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 5 x 10^-6) for pattern recognition memory (PRM) percent correct in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs4601609
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary