rs768119894
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs768119894(C;C) |
| Make rs768119894(C;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 7 |
| Position | 103636370 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs768119894 |
| dbSNP (classic) | rs768119894 |
| ClinGen | rs768119894 |
| ebi | rs768119894 |
| HLI | rs768119894 |
| Exac | rs768119894 |
| Gnomad | rs768119894 |
| Varsome | rs768119894 |
| LitVar | rs768119894 |
| Map | rs768119894 |
| PheGenI | rs768119894 |
| Biobank | rs768119894 |
| 1000 genomes | rs768119894 |
| hgdp | rs768119894 |
| ensembl | rs768119894 |
| geneview | rs768119894 |
| scholar | rs768119894 |
| rs768119894 | |
| pharmgkb | rs768119894 |
| gwascentral | rs768119894 |
| openSNP | rs768119894 |
| 23andMe | rs768119894 |
| SNPshot | rs768119894 |
| SNPdbe | rs768119894 |
| MSV3d | rs768119894 |
| GWAS Ctlg | rs768119894 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs768119894(C;C) |
| Alt | rs768119894(C;C) |
| Reference | Rs768119894(T;T) |
| Significance | Pathogenic |
| Disease | Epilepsy |
| Variation | info |
| Gene | RELN |
| CLNDBN | Epilepsy, familial temporal lobe, 7 |
| Reversed | 0 |
| HGVS | NC_000007.13:g.103276817T>C |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000194189.1, |
