rs10176705
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10176705(C;C) |
Make rs10176705(C;T) |
Make rs10176705(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 50517636 |
Gene | NRXN1 |
is a | snp |
is | mentioned by |
dbSNP | rs10176705 |
dbSNP (classic) | rs10176705 |
ClinGen | rs10176705 |
ebi | rs10176705 |
HLI | rs10176705 |
Exac | rs10176705 |
Gnomad | rs10176705 |
Varsome | rs10176705 |
LitVar | rs10176705 |
Map | rs10176705 |
PheGenI | rs10176705 |
Biobank | rs10176705 |
1000 genomes | rs10176705 |
hgdp | rs10176705 |
ensembl | rs10176705 |
geneview | rs10176705 |
scholar | rs10176705 |
rs10176705 | |
pharmgkb | rs10176705 |
gwascentral | rs10176705 |
openSNP | rs10176705 |
23andMe | rs10176705 |
SNPshot | rs10176705 |
SNPdbe | rs10176705 |
MSV3d | rs10176705 |
GWAS Ctlg | rs10176705 |
GMAF | 0.2484 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20691247] |
Trait | Personality |
Title | A genome-wide association study of Cloninger's temperament scales: Implications for the evolutionary genetics of personality |
Risk Allele | T |
P-val | 0.000009 |
Odds Ratio | 0.10 [NR] unit increase |