Rs10503887
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10503887 |
| PheGenI | rs10503887 |
| nextbio | rs10503887 |
| hapmap | rs10503887 |
| 1000 genomes | rs10503887 |
| hgdp | rs10503887 |
| ensembl | rs10503887 |
| gopubmed | rs10503887 |
| geneview | rs10503887 |
| scholar | rs10503887 |
| rs10503887 | |
| pharmgkb | rs10503887 |
| gwascentral | rs10503887 |
| openSNP | rs10503887 |
| 23andMe | rs10503887 |
| 23andMe all | rs10503887 |
| SNP Nexus | |
| SNPshot | rs10503887 |
| SNPdbe | rs10503887 |
| MSV3d | rs10503887 |
| Gene | NRG1 |
| Chromosome | 8 |
| Orientation | plus |
| GMAF | 0.1062 |
| Position | 31633447 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs10503887(G;T) |
| Make rs10503887(T;T) |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs10503887 |
| PubMedID | [PMID 17903296] |
| Condition | Hip geometry |
| Gene | NRG1 |
| Risk Allele | |
| pValue | 2.00E-007 |
| OR | NA |
| 95% CI | |
| GET Evidence | |
|---|---|
| rs10503887 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.078125 |
| summary | |
