rs1795648
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1795648(A;A) |
| Make rs1795648(A;G) |
| Make rs1795648(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 55537732 |
| Gene | ERC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1795648 |
| dbSNP (classic) | rs1795648 |
| ClinGen | rs1795648 |
| ebi | rs1795648 |
| HLI | rs1795648 |
| Exac | rs1795648 |
| Gnomad | rs1795648 |
| Varsome | rs1795648 |
| LitVar | rs1795648 |
| Map | rs1795648 |
| PheGenI | rs1795648 |
| Biobank | rs1795648 |
| 1000 genomes | rs1795648 |
| hgdp | rs1795648 |
| ensembl | rs1795648 |
| geneview | rs1795648 |
| scholar | rs1795648 |
| rs1795648 | |
| pharmgkb | rs1795648 |
| gwascentral | rs1795648 |
| openSNP | rs1795648 |
| 23andMe | rs1795648 |
| SNPshot | rs1795648 |
| SNPdbe | rs1795648 |
| MSV3d | rs1795648 |
| GWAS Ctlg | rs1795648 |
| GMAF | 0.3228 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21057379 ]
|
| Trait | |
| Title | Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | None None |
