Rs1412337
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1412337 |
| PheGenI | rs1412337 |
| nextbio | rs1412337 |
| hapmap | rs1412337 |
| 1000 genomes | rs1412337 |
| hgdp | rs1412337 |
| ensembl | rs1412337 |
| gopubmed | rs1412337 |
| geneview | rs1412337 |
| scholar | rs1412337 |
| rs1412337 | |
| pharmgkb | rs1412337 |
| gwascentral | rs1412337 |
| openSNP | rs1412337 |
| 23andMe | rs1412337 |
| 23andMe all | rs1412337 |
| SNP Nexus | |
| SNPshot | rs1412337 |
| SNPdbe | rs1412337 |
| MSV3d | rs1412337 |
| Chromosome | 1 |
| Orientation | minus |
| GMAF | 0.1951 |
| Position | 168618641 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1412337(C;C) |
| Make rs1412337(C;T) |
| Make rs1412337(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs1412337 |
| PubMedID | [PMID 17903295] |
| Condition | Morbidity-free survival |
| Gene | DPT |
| Risk Allele | |
| pValue | 2.00E-009 |
| OR | NA |
| 95% CI | |
| GET Evidence | |
|---|---|
| rs1412337 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.117188 |
| summary | |
