rs28939694
From SNPedia
| Merged into | rs121908982 |
| Orientation | minus |
| Stabilized | plus |
| Make rs28939694(C;C) |
| Make rs28939694(C;T) |
| Make rs28939694(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 2225526 |
| Gene | MAD1L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28939694 |
| dbSNP (classic) | rs28939694 |
| ClinGen | rs28939694 |
| ebi | rs28939694 |
| HLI | rs28939694 |
| Exac | rs28939694 |
| Gnomad | rs28939694 |
| Varsome | rs28939694 |
| LitVar | rs28939694 |
| Map | rs28939694 |
| PheGenI | rs28939694 |
| Biobank | rs28939694 |
| 1000 genomes | rs28939694 |
| hgdp | rs28939694 |
| ensembl | rs28939694 |
| geneview | rs28939694 |
| scholar | rs28939694 |
| rs28939694 | |
| pharmgkb | rs28939694 |
| gwascentral | rs28939694 |
| openSNP | rs28939694 |
| 23andMe | rs28939694 |
| SNPshot | rs28939694 |
| SNPdbe | rs28939694 |
| MSV3d | rs28939694 |
| GWAS Ctlg | rs28939694 |
| Status | Merged into rs121908982 |
| Max Magnitude | 0 |
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
