rs606231468
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs606231468(C;C) |
| Make rs606231468(C;T) |
| Make rs606231468(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 5 |
| Position | 161545228 |
| Gene | GABRB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs606231468 |
| dbSNP (classic) | rs606231468 |
| ClinGen | rs606231468 |
| ebi | rs606231468 |
| HLI | rs606231468 |
| Exac | rs606231468 |
| Gnomad | rs606231468 |
| Varsome | rs606231468 |
| LitVar | rs606231468 |
| Map | rs606231468 |
| PheGenI | rs606231468 |
| Biobank | rs606231468 |
| 1000 genomes | rs606231468 |
| hgdp | rs606231468 |
| ensembl | rs606231468 |
| geneview | rs606231468 |
| scholar | rs606231468 |
| rs606231468 | |
| pharmgkb | rs606231468 |
| gwascentral | rs606231468 |
| openSNP | rs606231468 |
| 23andMe | rs606231468 |
| SNPshot | rs606231468 |
| SNPdbe | rs606231468 |
| MSV3d | rs606231468 |
| GWAS Ctlg | rs606231468 |
| Max Magnitude | 0 |
aka NM_021911.2(GABRB2):c.236T>C or (p.Met79Thr)
OMIM pathogenic variant
