rs763818876
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs763818876(A;A) |
| Make rs763818876(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 1051775 |
| Gene | AGRN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs763818876 |
| dbSNP (classic) | rs763818876 |
| ClinGen | rs763818876 |
| ebi | rs763818876 |
| HLI | rs763818876 |
| Exac | rs763818876 |
| Gnomad | rs763818876 |
| Varsome | rs763818876 |
| LitVar | rs763818876 |
| Map | rs763818876 |
| PheGenI | rs763818876 |
| Biobank | rs763818876 |
| 1000 genomes | rs763818876 |
| hgdp | rs763818876 |
| ensembl | rs763818876 |
| geneview | rs763818876 |
| scholar | rs763818876 |
| rs763818876 | |
| pharmgkb | rs763818876 |
| gwascentral | rs763818876 |
| openSNP | rs763818876 |
| 23andMe | rs763818876 |
| SNPshot | rs763818876 |
| SNPdbe | rs763818876 |
| MSV3d | rs763818876 |
| GWAS Ctlg | rs763818876 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs763818876(A;A) |
| Alt | rs763818876(A;A) |
| Reference | Rs763818876(G;G) |
| Significance | Pathogenic |
| Disease | Congenital myasthenic syndrome |
| Variation | info |
| Gene | AGRN |
| CLNDBN | Congenital myasthenic syndrome |
| Reversed | 0 |
| HGVS | NC_000001.10:g.987155G>A |
| CLNSRC | |
| CLNACC | RCV000235024.1, |
