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rs4668356

From SNPedia

Orientationplus
Stabilizedplus
Make rs4668356(C;C)
Make rs4668356(C;T)
Make rs4668356(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position170965956
GeneGORASP2
is asnp
is mentioned by
dbSNPrs4668356
ebirs4668356
HLIrs4668356
Exacrs4668356
Varsomers4668356
Maprs4668356
PheGenIrs4668356
hapmaprs4668356
1000 genomesrs4668356
hgdprs4668356
ensemblrs4668356
gopubmedrs4668356
geneviewrs4668356
scholarrs4668356
googlers4668356
pharmgkbrs4668356
gwascentralrs4668356
openSNPrs4668356
23andMers4668356
23andMe allrs4668356
SNP Nexus

SNPshotrs4668356
SNPdbers4668356
MSV3drs4668356
GWAS Ctlgrs4668356
GMAF0.141
Max Magnitude
? (C;C) (C;T) (T;T) 28

Mentioned in retracted [PMID 20595579]

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, hit (p = 1 x 10^-6) for paired associates learning (PAL) total errors at 8 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery


GET Evidence
rs4668356
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.81465
summary