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rs1820460

From SNPedia

Orientationplus
Stabilizedplus
Make rs1820460(A;A)
Make rs1820460(A;C)
Make rs1820460(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position107310928
is asnp
is mentioned by
dbSNPrs1820460
dbSNP (classic)rs1820460
ClinGenrs1820460
ebirs1820460
HLIrs1820460
Exacrs1820460
Gnomadrs1820460
Varsomers1820460
LitVarrs1820460
Maprs1820460
PheGenIrs1820460
Biobankrs1820460
1000 genomesrs1820460
hgdprs1820460
ensemblrs1820460
geneviewrs1820460
scholarrs1820460
googlers1820460
pharmgkbrs1820460
gwascentralrs1820460
openSNPrs1820460
23andMers1820460
SNPshotrs1820460
SNPdbers1820460
MSV3drs1820460
GWAS Ctlgrs1820460
GMAF0.2952
Max Magnitude0
? (A;A) (A;C) (C;C) 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