rs77244975
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs77244975(C;C) |
| Make rs77244975(C;T) |
| Make rs77244975(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 10 |
| Position | 67448217 |
| Gene | CTNNA3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs77244975 |
| dbSNP (classic) | rs77244975 |
| ClinGen | rs77244975 |
| ebi | rs77244975 |
| HLI | rs77244975 |
| Exac | rs77244975 |
| Gnomad | rs77244975 |
| Varsome | rs77244975 |
| LitVar | rs77244975 |
| Map | rs77244975 |
| PheGenI | rs77244975 |
| Biobank | rs77244975 |
| 1000 genomes | rs77244975 |
| hgdp | rs77244975 |
| ensembl | rs77244975 |
| geneview | rs77244975 |
| scholar | rs77244975 |
| rs77244975 | |
| pharmgkb | rs77244975 |
| gwascentral | rs77244975 |
| openSNP | rs77244975 |
| 23andMe | rs77244975 |
| SNPshot | rs77244975 |
| SNPdbe | rs77244975 |
| MSV3d | rs77244975 |
| GWAS Ctlg | rs77244975 |
| Max Magnitude | 0 |
[PMID 26507551
] Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome
