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rs9320913

From SNPedia

Orientationplus
Stabilizedplus
Make rs9320913(A;A)
Make rs9320913(A;C)
Make rs9320913(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position98136857
is asnp
is mentioned by
dbSNPrs9320913
dbSNP (classic)rs9320913
ClinGenrs9320913
ebirs9320913
HLIrs9320913
Exacrs9320913
Gnomadrs9320913
Varsomers9320913
LitVarrs9320913
Maprs9320913
PheGenIrs9320913
Biobankrs9320913
1000 genomesrs9320913
hgdprs9320913
ensemblrs9320913
geneviewrs9320913
scholarrs9320913
googlers9320913
pharmgkbrs9320913
gwascentralrs9320913
openSNPrs9320913
23andMers9320913
SNPshotrs9320913
SNPdbers9320913
MSV3drs9320913
GWAS Ctlgrs9320913
GMAF0.3871
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 28530673OA-icon.png] Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence.

GWAS snp
PMID [PMID 23722424OA-icon.png]
Trait Educational attainment
Title GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Risk Allele A
P-val 4E-10
Odds Ratio .10 [NR] unit increase