rs201044262
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs201044262(A;A) |
| Make rs201044262(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 7 |
| Position | 103640597 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201044262 |
| dbSNP (classic) | rs201044262 |
| ClinGen | rs201044262 |
| ebi | rs201044262 |
| HLI | rs201044262 |
| Exac | rs201044262 |
| Gnomad | rs201044262 |
| Varsome | rs201044262 |
| LitVar | rs201044262 |
| Map | rs201044262 |
| PheGenI | rs201044262 |
| Biobank | rs201044262 |
| 1000 genomes | rs201044262 |
| hgdp | rs201044262 |
| ensembl | rs201044262 |
| geneview | rs201044262 |
| scholar | rs201044262 |
| rs201044262 | |
| pharmgkb | rs201044262 |
| gwascentral | rs201044262 |
| openSNP | rs201044262 |
| 23andMe | rs201044262 |
| SNPshot | rs201044262 |
| SNPdbe | rs201044262 |
| MSV3d | rs201044262 |
| GWAS Ctlg | rs201044262 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201044262(A;A) |
| Alt | rs201044262(A;A) |
| Reference | Rs201044262(G;G) |
| Significance | Pathogenic |
| Disease | Epilepsy |
| Variation | info |
| Gene | RELN |
| CLNDBN | Epilepsy, familial temporal lobe, 7 |
| Reversed | 0 |
| HGVS | NC_000007.13:g.103281044G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000193679.1, |
