rs1057521979
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Make rs1057521979(C;C) | 
| Make rs1057521979(C;T) | 
| Reference | GRCh38.p7 38.3/150 | 
| Chromosome | 5 | 
| Position | 161411034 | 
| Gene | GABRB2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs1057521979 | 
| dbSNP (classic) | rs1057521979 | 
| ClinGen | rs1057521979 | 
| ebi | rs1057521979 | 
| HLI | rs1057521979 | 
| Exac | rs1057521979 | 
| Gnomad | rs1057521979 | 
| Varsome | rs1057521979 | 
| LitVar | rs1057521979 | 
| Map | rs1057521979 | 
| PheGenI | rs1057521979 | 
| Biobank | rs1057521979 | 
| 1000 genomes | rs1057521979 | 
| hgdp | rs1057521979 | 
| ensembl | rs1057521979 | 
| geneview | rs1057521979 | 
| scholar | rs1057521979 | 
| rs1057521979 | |
| pharmgkb | rs1057521979 | 
| gwascentral | rs1057521979 | 
| openSNP | rs1057521979 | 
| 23andMe | rs1057521979 | 
| SNPshot | rs1057521979 | 
| SNPdbe | rs1057521979 | 
| MSV3d | rs1057521979 | 
| GWAS Ctlg | rs1057521979 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs1057521979(C;C) | 
| Alt | rs1057521979(C;C) | 
| Reference | Rs1057521979(T;T) | 
| Significance | Probable-Pathogenic | 
| Disease | not provided | 
| Variation | info | 
| Gene | GABRB2 | 
| CLNDBN | not provided | 
| Reversed | 1 | 
| HGVS | NC_000005.9:g.160838040A>G | 
| CLNSRC | |
| CLNACC | RCV000439405.1, | 
