rs781028867
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs781028867(C;T) |
| Make rs781028867(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 16 |
| Position | 53873846 |
| Gene | FTO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs781028867 |
| dbSNP (classic) | rs781028867 |
| ClinGen | rs781028867 |
| ebi | rs781028867 |
| HLI | rs781028867 |
| Exac | rs781028867 |
| Gnomad | rs781028867 |
| Varsome | rs781028867 |
| LitVar | rs781028867 |
| Map | rs781028867 |
| PheGenI | rs781028867 |
| Biobank | rs781028867 |
| 1000 genomes | rs781028867 |
| hgdp | rs781028867 |
| ensembl | rs781028867 |
| geneview | rs781028867 |
| scholar | rs781028867 |
| rs781028867 | |
| pharmgkb | rs781028867 |
| gwascentral | rs781028867 |
| openSNP | rs781028867 |
| 23andMe | rs781028867 |
| SNPshot | rs781028867 |
| SNPdbe | rs781028867 |
| MSV3d | rs781028867 |
| GWAS Ctlg | rs781028867 |
| Max Magnitude | 0 |
aka NM_001080432.2(FTO):c.956C>T or (p.Ser319Phe)
OMIM pathogenic variant
