rs1049623
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1049623(A;A) |
| Make rs1049623(A;G) |
| Make rs1049623(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 30897052 |
| Gene | DDR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1049623 |
| dbSNP (classic) | rs1049623 |
| ClinGen | rs1049623 |
| ebi | rs1049623 |
| HLI | rs1049623 |
| Exac | rs1049623 |
| Gnomad | rs1049623 |
| Varsome | rs1049623 |
| LitVar | rs1049623 |
| Map | rs1049623 |
| PheGenI | rs1049623 |
| Biobank | rs1049623 |
| 1000 genomes | rs1049623 |
| hgdp | rs1049623 |
| ensembl | rs1049623 |
| geneview | rs1049623 |
| scholar | rs1049623 |
| rs1049623 | |
| pharmgkb | rs1049623 |
| gwascentral | rs1049623 |
| openSNP | rs1049623 |
| 23andMe | rs1049623 |
| SNPshot | rs1049623 |
| SNPdbe | rs1049623 |
| MSV3d | rs1049623 |
| GWAS Ctlg | rs1049623 |
| GMAF | 0.4927 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 17440435] schizophrenia rs1049623 associated with schizophrenia (odds ratio=1.44, 95% confidence interval: 1.15-1.79, adjusted P=0.0016).
[PMID 17440435] schizophrenia the SNPs (rs1049623, rs2267641 and rs2239518) haplotype remaining significant even after adjustment for multiple testing (adjusted P=0.0136).
[PMID 27718532] Identification of miRSNPs associated with the risk of multiple myeloma.
