rs16887244
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16887244(A;A) |
| Make rs16887244(A;G) |
| Make rs16887244(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 38173827 |
| Gene | LSM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16887244 |
| dbSNP (classic) | rs16887244 |
| ClinGen | rs16887244 |
| ebi | rs16887244 |
| HLI | rs16887244 |
| Exac | rs16887244 |
| Gnomad | rs16887244 |
| Varsome | rs16887244 |
| LitVar | rs16887244 |
| Map | rs16887244 |
| PheGenI | rs16887244 |
| Biobank | rs16887244 |
| 1000 genomes | rs16887244 |
| hgdp | rs16887244 |
| ensembl | rs16887244 |
| geneview | rs16887244 |
| scholar | rs16887244 |
| rs16887244 | |
| pharmgkb | rs16887244 |
| gwascentral | rs16887244 |
| openSNP | rs16887244 |
| 23andMe | rs16887244 |
| SNPshot | rs16887244 |
| SNPdbe | rs16887244 |
| MSV3d | rs16887244 |
| GWAS Ctlg | rs16887244 |
| GMAF | 0.2466 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22037555 ]
|
| Trait | |
| Title | Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. |
| Risk Allele | |
| P-val | 1E-10 |
| Odds Ratio | 1.1900 None |
