rs2267641
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2267641(A;A) |
| Make rs2267641(A;C) |
| Make rs2267641(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 30897427 |
| Gene | DDR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2267641 |
| dbSNP (classic) | rs2267641 |
| ClinGen | rs2267641 |
| ebi | rs2267641 |
| HLI | rs2267641 |
| Exac | rs2267641 |
| Gnomad | rs2267641 |
| Varsome | rs2267641 |
| LitVar | rs2267641 |
| Map | rs2267641 |
| PheGenI | rs2267641 |
| Biobank | rs2267641 |
| 1000 genomes | rs2267641 |
| hgdp | rs2267641 |
| ensembl | rs2267641 |
| geneview | rs2267641 |
| scholar | rs2267641 |
| rs2267641 | |
| pharmgkb | rs2267641 |
| gwascentral | rs2267641 |
| openSNP | rs2267641 |
| 23andMe | rs2267641 |
| SNPshot | rs2267641 |
| SNPdbe | rs2267641 |
| MSV3d | rs2267641 |
| GWAS Ctlg | rs2267641 |
| GMAF | 0.2392 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 17440435] schizophrenia the SNPs (rs1049623, rs2267641 and rs2239518) haplotype remaining significant even after adjustment for multiple testing (adjusted P=0.0136).
[PMID 20182441] Genetic Variants of the DDR1 Gene Are Associated with Vitiligo in Two Independent Brazilian Population Samples
[PMID 20372823] Linkage and association study of discoidin domain receptor 1 as a novel susceptibility gene for childhood IgA nephropathy.
[PMID 22077590] The discoidin domain receptor 1 gene has a functional A2RE sequence.
