rs28379706
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs28379706(C;C) |
Make rs28379706(C;T) |
Make rs28379706(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 22 |
Position | 50289633 |
Gene | PLXNB2 |
is a | snp |
is | mentioned by |
dbSNP | rs28379706 |
dbSNP (classic) | rs28379706 |
ClinGen | rs28379706 |
ebi | rs28379706 |
HLI | rs28379706 |
Exac | rs28379706 |
Gnomad | rs28379706 |
Varsome | rs28379706 |
LitVar | rs28379706 |
Map | rs28379706 |
PheGenI | rs28379706 |
Biobank | rs28379706 |
1000 genomes | rs28379706 |
hgdp | rs28379706 |
ensembl | rs28379706 |
geneview | rs28379706 |
scholar | rs28379706 |
rs28379706 | |
pharmgkb | rs28379706 |
gwascentral | rs28379706 |
openSNP | rs28379706 |
23andMe | rs28379706 |
SNPshot | rs28379706 |
SNPdbe | rs28379706 |
MSV3d | rs28379706 |
GWAS Ctlg | rs28379706 |
Max Magnitude | 0 |
Using a sample of extremely intelligent adolescents in comparison to a group of more typically intelligent people, it was found that the C allele of this SNP increased IQ and explained 0.16% of the variance in IQ.
http://www.nature.com/mp/journal/vaop/ncurrent/full/mp2015108a.html