rs587777927
From SNPedia
| Merged into | rs121908808 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs587777927(-;T) |
| Make rs587777927(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 7 |
| Position | 117652853 |
| Gene | CFTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs587777927 |
| dbSNP (classic) | rs587777927 |
| ClinGen | rs587777927 |
| ebi | rs587777927 |
| HLI | rs587777927 |
| Exac | rs587777927 |
| Gnomad | rs587777927 |
| Varsome | rs587777927 |
| LitVar | rs587777927 |
| Map | rs587777927 |
| PheGenI | rs587777927 |
| Biobank | rs587777927 |
| 1000 genomes | rs587777927 |
| hgdp | rs587777927 |
| ensembl | rs587777927 |
| geneview | rs587777927 |
| scholar | rs587777927 |
| rs587777927 | |
| pharmgkb | rs587777927 |
| gwascentral | rs587777927 |
| openSNP | rs587777927 |
| 23andMe | rs587777927 |
| SNPshot | rs587777927 |
| SNPdbe | rs587777927 |
| MSV3d | rs587777927 |
| GWAS Ctlg | rs587777927 |
| Status | Merged into rs121908808 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs587777927(T;T) |
| Alt | rs587777927(T;T) |
| Reference | Rs587777927(;) |
| Significance | Pathogenic |
| Disease | Cystic fibrosis |
| Variation | info |
| Gene | CFTR |
| CLNDBN | Cystic fibrosis |
| Reversed | 0 |
| HGVS | NC_000007.13:g.117292911dupT |
| CLNSRC | CFTR2 |
| CLNACC | RCV000047018.4, |
