rs76822696
From SNPedia
| Merged into | rs62526245 |
| Orientation | plus |
| Make rs76822696(A;A) |
| Make rs76822696(A;C) |
| Make rs76822696(C;C) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 8 |
| Position | 84016901 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76822696 |
| dbSNP (classic) | rs76822696 |
| ClinGen | rs76822696 |
| ebi | rs76822696 |
| HLI | rs76822696 |
| Exac | rs76822696 |
| Gnomad | rs76822696 |
| Varsome | rs76822696 |
| LitVar | rs76822696 |
| Map | rs76822696 |
| PheGenI | rs76822696 |
| Biobank | rs76822696 |
| 1000 genomes | rs76822696 |
| hgdp | rs76822696 |
| ensembl | rs76822696 |
| geneview | rs76822696 |
| scholar | rs76822696 |
| rs76822696 | |
| pharmgkb | rs76822696 |
| gwascentral | rs76822696 |
| openSNP | rs76822696 |
| 23andMe | rs76822696 |
| SNPshot | rs76822696 |
| SNPdbe | rs76822696 |
| MSV3d | rs76822696 |
| GWAS Ctlg | rs76822696 |
| Status | Merged into rs62526245 |
| Max Magnitude | 0 |
[PMID 26507551
] Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome
