rs922847767
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs922847767(C;C) |
| Make rs922847767(C;T) |
| Make rs922847767(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 9 |
| Position | 98371535 |
| Gene | GABBR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs922847767 |
| dbSNP (classic) | rs922847767 |
| ClinGen | rs922847767 |
| ebi | rs922847767 |
| HLI | rs922847767 |
| Exac | rs922847767 |
| Gnomad | rs922847767 |
| Varsome | rs922847767 |
| LitVar | rs922847767 |
| Map | rs922847767 |
| PheGenI | rs922847767 |
| Biobank | rs922847767 |
| 1000 genomes | rs922847767 |
| hgdp | rs922847767 |
| ensembl | rs922847767 |
| geneview | rs922847767 |
| scholar | rs922847767 |
| rs922847767 | |
| pharmgkb | rs922847767 |
| gwascentral | rs922847767 |
| openSNP | rs922847767 |
| 23andMe | rs922847767 |
| SNPshot | rs922847767 |
| SNPdbe | rs922847767 |
| MSV3d | rs922847767 |
| GWAS Ctlg | rs922847767 |
| Max Magnitude | 0 |
aka NM_005458.7(GABBR2):c.1699G>A or (p.Ala567Thr)
OMIM pathogenic variant
