rs362719
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs362719(A;A) |
| Make rs362719(A;C) |
| Make rs362719(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 103545430 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs362719 |
| dbSNP (classic) | rs362719 |
| ClinGen | rs362719 |
| ebi | rs362719 |
| HLI | rs362719 |
| Exac | rs362719 |
| Gnomad | rs362719 |
| Varsome | rs362719 |
| LitVar | rs362719 |
| Map | rs362719 |
| PheGenI | rs362719 |
| Biobank | rs362719 |
| 1000 genomes | rs362719 |
| hgdp | rs362719 |
| ensembl | rs362719 |
| geneview | rs362719 |
| scholar | rs362719 |
| rs362719 | |
| pharmgkb | rs362719 |
| gwascentral | rs362719 |
| openSNP | rs362719 |
| 23andMe | rs362719 |
| SNPshot | rs362719 |
| SNPdbe | rs362719 |
| MSV3d | rs362719 |
| GWAS Ctlg | rs362719 |
| GMAF | 0.3439 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21863557] A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han
[PMID 18597938] Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
[PMID 19691043
] Sex-specific association of the Reelin gene with bipolar disorder.
