rs1256531
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 |
Make rs1256531(A;G) |
Make rs1256531(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 65281041 |
Gene | PTBP1P |
is a | snp |
is | mentioned by |
dbSNP | rs1256531 |
dbSNP (classic) | rs1256531 |
ClinGen | rs1256531 |
ebi | rs1256531 |
HLI | rs1256531 |
Exac | rs1256531 |
Gnomad | rs1256531 |
Varsome | rs1256531 |
LitVar | rs1256531 |
Map | rs1256531 |
PheGenI | rs1256531 |
Biobank | rs1256531 |
1000 genomes | rs1256531 |
hgdp | rs1256531 |
ensembl | rs1256531 |
geneview | rs1256531 |
scholar | rs1256531 |
rs1256531 | |
pharmgkb | rs1256531 |
gwascentral | rs1256531 |
openSNP | rs1256531 |
23andMe | rs1256531 |
SNPshot | rs1256531 |
SNPdbe | rs1256531 |
MSV3d | rs1256531 |
GWAS Ctlg | rs1256531 |
GMAF | 0.2466 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324] |
Trait | Conduct disorder (symptom count) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | 0.09 [NR] unit increase |