rs121434579
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in complete genomics | 
| Make rs121434579(A;A) | 
| Make rs121434579(A;C) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 5 | 
| Position | 161895774 | 
| Gene | GABRA1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs121434579 | 
| dbSNP (classic) | rs121434579 | 
| ClinGen | rs121434579 | 
| ebi | rs121434579 | 
| HLI | rs121434579 | 
| Exac | rs121434579 | 
| Gnomad | rs121434579 | 
| Varsome | rs121434579 | 
| LitVar | rs121434579 | 
| Map | rs121434579 | 
| PheGenI | rs121434579 | 
| Biobank | rs121434579 | 
| 1000 genomes | rs121434579 | 
| hgdp | rs121434579 | 
| ensembl | rs121434579 | 
| geneview | rs121434579 | 
| scholar | rs121434579 | 
| rs121434579 | |
| pharmgkb | rs121434579 | 
| gwascentral | rs121434579 | 
| openSNP | rs121434579 | 
| 23andMe | rs121434579 | 
| SNPshot | rs121434579 | 
| SNPdbe | rs121434579 | 
| MSV3d | rs121434579 | 
| GWAS Ctlg | rs121434579 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs121434579(A;A) | 
| Alt | rs121434579(A;A) | 
| Reference | Rs121434579(C;C) | 
| Significance | Other | 
| Disease | Epilepsy | 
| Variation | info | 
| Gene | GABRA1 | 
| CLNDBN | Epilepsy, juvenile myoclonic 5 | 
| Reversed | 0 | 
| HGVS | NC_000005.9:g.161322780C>A | 
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) | 
| CLNACC | RCV000017601.4, | 


