rs10487372
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs10487372(C;T) |
| Make rs10487372(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117560845 |
| Gene | CFTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10487372 |
| dbSNP (classic) | rs10487372 |
| ClinGen | rs10487372 |
| ebi | rs10487372 |
| HLI | rs10487372 |
| Exac | rs10487372 |
| Gnomad | rs10487372 |
| Varsome | rs10487372 |
| LitVar | rs10487372 |
| Map | rs10487372 |
| PheGenI | rs10487372 |
| Biobank | rs10487372 |
| 1000 genomes | rs10487372 |
| hgdp | rs10487372 |
| ensembl | rs10487372 |
| geneview | rs10487372 |
| scholar | rs10487372 |
| rs10487372 | |
| pharmgkb | rs10487372 |
| gwascentral | rs10487372 |
| openSNP | rs10487372 |
| 23andMe | rs10487372 |
| SNPshot | rs10487372 |
| SNPdbe | rs10487372 |
| MSV3d | rs10487372 |
| GWAS Ctlg | rs10487372 |
| GMAF | 0.1079 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20116881
] Cystic fibrosis transmembrane conductance regulator gene mutation and lung cancer risk
