rs121908762
From SNPedia
| Merged into | rs121908761 |
| Orientation | plus |
| Stabilized | plus |
| Make rs121908762(A;A) |
| Make rs121908762(A;C) |
| Make rs121908762(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117611717 |
| Gene | CFTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121908762 |
| dbSNP (classic) | rs121908762 |
| ClinGen | rs121908762 |
| ebi | rs121908762 |
| HLI | rs121908762 |
| Exac | rs121908762 |
| Gnomad | rs121908762 |
| Varsome | rs121908762 |
| LitVar | rs121908762 |
| Map | rs121908762 |
| PheGenI | rs121908762 |
| Biobank | rs121908762 |
| 1000 genomes | rs121908762 |
| hgdp | rs121908762 |
| ensembl | rs121908762 |
| geneview | rs121908762 |
| scholar | rs121908762 |
| rs121908762 | |
| pharmgkb | rs121908762 |
| gwascentral | rs121908762 |
| openSNP | rs121908762 |
| 23andMe | rs121908762 |
| SNPshot | rs121908762 |
| SNPdbe | rs121908762 |
| MSV3d | rs121908762 |
| GWAS Ctlg | rs121908762 |
| Status | Merged into rs121908761 |
| Max Magnitude | 0 |
[PMID 15948195] Mutation spectrum in Jewish cystic fibrosis patients in Israel: implication to carrier screening.
