rs144261491
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs144261491(C;C) |
| Make rs144261491(C;T) |
| Make rs144261491(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 5 |
| Position | 88838104 |
| Gene | MEF2C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs144261491 |
| dbSNP (classic) | rs144261491 |
| ClinGen | rs144261491 |
| ebi | rs144261491 |
| HLI | rs144261491 |
| Exac | rs144261491 |
| Gnomad | rs144261491 |
| Varsome | rs144261491 |
| LitVar | rs144261491 |
| Map | rs144261491 |
| PheGenI | rs144261491 |
| Biobank | rs144261491 |
| 1000 genomes | rs144261491 |
| hgdp | rs144261491 |
| ensembl | rs144261491 |
| geneview | rs144261491 |
| scholar | rs144261491 |
| rs144261491 | |
| pharmgkb | rs144261491 |
| gwascentral | rs144261491 |
| openSNP | rs144261491 |
| 23andMe | rs144261491 |
| SNPshot | rs144261491 |
| SNPdbe | rs144261491 |
| MSV3d | rs144261491 |
| GWAS Ctlg | rs144261491 |
| Max Magnitude | 0 |
Said to be an "Amerindian-specific variant" in [PMID 26805783
]; specifically, the allele frequency for the minor (T) allele is around 4% in many South American populations but is undetected in Asian, European and African populations.
