rs878854144
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in clinvar | 
| Make rs878854144(-;-) | 
| Make rs878854144(-;G) | 
| Reference | GRCh38.p2 38.2/147 | 
| Chromosome | 5 | 
| Position | 162097840 | 
| Gene | GABRG2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs878854144 | 
| dbSNP (classic) | rs878854144 | 
| ClinGen | rs878854144 | 
| ebi | rs878854144 | 
| HLI | rs878854144 | 
| Exac | rs878854144 | 
| Gnomad | rs878854144 | 
| Varsome | rs878854144 | 
| LitVar | rs878854144 | 
| Map | rs878854144 | 
| PheGenI | rs878854144 | 
| Biobank | rs878854144 | 
| 1000 genomes | rs878854144 | 
| hgdp | rs878854144 | 
| ensembl | rs878854144 | 
| geneview | rs878854144 | 
| scholar | rs878854144 | 
| rs878854144 | |
| pharmgkb | rs878854144 | 
| gwascentral | rs878854144 | 
| openSNP | rs878854144 | 
| 23andMe | rs878854144 | 
| SNPshot | rs878854144 | 
| SNPdbe | rs878854144 | 
| MSV3d | rs878854144 | 
| GWAS Ctlg | rs878854144 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs878854144(-;-) | 
| Alt | rs878854144(-;-) | 
| Reference | Rs878854144(G;G) | 
| Significance | Pathogenic | 
| Disease | Epilepsy Familial febrile seizures 8 | 
| Variation | info | 
| Gene | GABRG2 | 
| CLNDBN | Epilepsy, childhood absence 2 Familial febrile seizures 8 | 
| Reversed | 0 | 
| HGVS | NC_000005.9:g.161524846delG | 
| CLNSRC | |
| CLNACC | RCV000227482.2, | 
