Rs151222
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs151222 |
| PheGenI | rs151222 |
| nextbio | rs151222 |
| hapmap | rs151222 |
| 1000 genomes | rs151222 |
| hgdp | rs151222 |
| ensembl | rs151222 |
| gopubmed | rs151222 |
| geneview | rs151222 |
| scholar | rs151222 |
| rs151222 | |
| pharmgkb | rs151222 |
| gwascentral | rs151222 |
| openSNP | rs151222 |
| 23andMe | rs151222 |
| 23andMe all | rs151222 |
| SNP Nexus | |
| SNPshot | rs151222 |
| SNPdbe | rs151222 |
| MSV3d | rs151222 |
| Gene | ACSM1 |
| Chromosome | 16 |
| Orientation | plus |
| GMAF | 0.0902 |
| Position | 20674492 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs151222(C;C) |
| Make rs151222(C;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs151222 |
| PubMedID | [PMID 18347602] |
| Condition | Schizophrenia |
| Gene | ACSM1, BUCS1 |
| Risk Allele | |
| pValue | 6.00E-006 |
| OR | 2.1 |
| 95% CI | |
[PMID 19197363] A genome-wide investigation of SNPs and CNVs in schizophrenia.
| GET Evidence | |
|---|---|
| rs151222 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.0703125 |
| summary | |
