rs61757459
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs61757459(A;A) |
| Make rs61757459(A;G) |
| Make rs61757459(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 94497767 |
| Gene | SERPINA12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61757459 |
| dbSNP (classic) | rs61757459 |
| ClinGen | rs61757459 |
| ebi | rs61757459 |
| HLI | rs61757459 |
| Exac | rs61757459 |
| Gnomad | rs61757459 |
| Varsome | rs61757459 |
| LitVar | rs61757459 |
| Map | rs61757459 |
| PheGenI | rs61757459 |
| Biobank | rs61757459 |
| 1000 genomes | rs61757459 |
| hgdp | rs61757459 |
| ensembl | rs61757459 |
| geneview | rs61757459 |
| scholar | rs61757459 |
| rs61757459 | |
| pharmgkb | rs61757459 |
| gwascentral | rs61757459 |
| openSNP | rs61757459 |
| 23andMe | rs61757459 |
| SNPshot | rs61757459 |
| SNPdbe | rs61757459 |
| MSV3d | rs61757459 |
| GWAS Ctlg | rs61757459 |
| Max Magnitude | 0 |
[PMID 23756768] Analysis of a rare functional truncating mutation rs61757459 in vaspin (SERPINA12) on circulating vaspin levels
