rs16902460
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs16902460(A;A) |
Make rs16902460(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 127907951 |
Gene | PVT1 |
is a | snp |
is | mentioned by |
dbSNP | rs16902460 |
dbSNP (classic) | rs16902460 |
ClinGen | rs16902460 |
ebi | rs16902460 |
HLI | rs16902460 |
Exac | rs16902460 |
Gnomad | rs16902460 |
Varsome | rs16902460 |
LitVar | rs16902460 |
Map | rs16902460 |
PheGenI | rs16902460 |
Biobank | rs16902460 |
1000 genomes | rs16902460 |
hgdp | rs16902460 |
ensembl | rs16902460 |
geneview | rs16902460 |
scholar | rs16902460 |
rs16902460 | |
pharmgkb | rs16902460 |
gwascentral | rs16902460 |
openSNP | rs16902460 |
23andMe | rs16902460 |
SNPshot | rs16902460 |
SNPdbe | rs16902460 |
MSV3d | rs16902460 |
GWAS Ctlg | rs16902460 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24132900] |
Trait | Psychosis (atypical) |
Title | Genome-wide association study of atypical psychosis. |
Risk Allele | |
P-val | 3E-6 |
Odds Ratio | NR NR |