rs117672662
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs117672662(C;C) |
| Make rs117672662(C;T) |
| Make rs117672662(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 14 |
| Position | 68958750 |
| Gene | ACTN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs117672662 |
| dbSNP (classic) | rs117672662 |
| ClinGen | rs117672662 |
| ebi | rs117672662 |
| HLI | rs117672662 |
| Exac | rs117672662 |
| Gnomad | rs117672662 |
| Varsome | rs117672662 |
| LitVar | rs117672662 |
| Map | rs117672662 |
| PheGenI | rs117672662 |
| Biobank | rs117672662 |
| 1000 genomes | rs117672662 |
| hgdp | rs117672662 |
| ensembl | rs117672662 |
| geneview | rs117672662 |
| scholar | rs117672662 |
| rs117672662 | |
| pharmgkb | rs117672662 |
| gwascentral | rs117672662 |
| openSNP | rs117672662 |
| 23andMe | rs117672662 |
| SNPshot | rs117672662 |
| SNPdbe | rs117672662 |
| MSV3d | rs117672662 |
| GWAS Ctlg | rs117672662 |
| Max Magnitude | 0 |
Said to be an "Amerindian-specific variant" in [PMID 26805783
]; specifically, the allele frequency for the minor (C) allele is around 7% in many South American populations but is either undetected or under 1% in Asian, European and African populations.
