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rs7662358

From SNPedia

Orientationplus
Stabilizedplus
Make rs7662358(A;A)
Make rs7662358(A;C)
Make rs7662358(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position188669705
is asnp
is mentioned by
dbSNPrs7662358
ebirs7662358
HLIrs7662358
Exacrs7662358
Varsomers7662358
Maprs7662358
PheGenIrs7662358
hapmaprs7662358
1000 genomesrs7662358
hgdprs7662358
ensemblrs7662358
gopubmedrs7662358
geneviewrs7662358
scholarrs7662358
googlers7662358
pharmgkbrs7662358
gwascentralrs7662358
openSNPrs7662358
23andMers7662358
23andMe allrs7662358
SNP Nexus

SNPshotrs7662358
SNPdbers7662358
MSV3drs7662358
GWAS Ctlgrs7662358
GMAF0.1373
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive performance
Title Common genetic variation and performance on standardized cognitive tests.
Risk Allele
P-val 9E-6
Odds Ratio NR NR