rs2073559
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2073559(C;C) |
| Make rs2073559(C;T) |
| Make rs2073559(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 103678477 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2073559 |
| dbSNP (classic) | rs2073559 |
| ClinGen | rs2073559 |
| ebi | rs2073559 |
| HLI | rs2073559 |
| Exac | rs2073559 |
| Gnomad | rs2073559 |
| Varsome | rs2073559 |
| LitVar | rs2073559 |
| Map | rs2073559 |
| PheGenI | rs2073559 |
| Biobank | rs2073559 |
| 1000 genomes | rs2073559 |
| hgdp | rs2073559 |
| ensembl | rs2073559 |
| geneview | rs2073559 |
| scholar | rs2073559 |
| rs2073559 | |
| pharmgkb | rs2073559 |
| gwascentral | rs2073559 |
| openSNP | rs2073559 |
| 23andMe | rs2073559 |
| SNPshot | rs2073559 |
| SNPdbe | rs2073559 |
| MSV3d | rs2073559 |
| GWAS Ctlg | rs2073559 |
| GMAF | 0.472 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20554015] No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population
[PMID 17621165] Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.
