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rs6486986

From SNPedia

Orientationplus
Stabilizedplus
Make rs6486986(G;G)
Make rs6486986(G;T)
Make rs6486986(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position19648661
GeneLOC101928387
is asnp
is mentioned by
dbSNPrs6486986
ebirs6486986
HLIrs6486986
Exacrs6486986
Varsomers6486986
Maprs6486986
PheGenIrs6486986
hapmaprs6486986
1000 genomesrs6486986
hgdprs6486986
ensemblrs6486986
gopubmedrs6486986
geneviewrs6486986
scholarrs6486986
googlers6486986
pharmgkbrs6486986
gwascentralrs6486986
openSNPrs6486986
23andMers6486986
23andMe allrs6486986
SNP Nexus

SNPshotrs6486986
SNPdbers6486986
MSV3drs6486986
GWAS Ctlgrs6486986
GMAF0.2378
Max Magnitude
? (G;G) (G;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.
Risk Allele
P-val 8E-6
Odds Ratio NR NR