rs10234329
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs10234329(A;C) |
| Make rs10234329(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117668151 |
| Gene | CFTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10234329 |
| dbSNP (classic) | rs10234329 |
| ClinGen | rs10234329 |
| ebi | rs10234329 |
| HLI | rs10234329 |
| Exac | rs10234329 |
| Gnomad | rs10234329 |
| Varsome | rs10234329 |
| LitVar | rs10234329 |
| Map | rs10234329 |
| PheGenI | rs10234329 |
| Biobank | rs10234329 |
| 1000 genomes | rs10234329 |
| hgdp | rs10234329 |
| ensembl | rs10234329 |
| geneview | rs10234329 |
| scholar | rs10234329 |
| rs10234329 | |
| pharmgkb | rs10234329 |
| gwascentral | rs10234329 |
| openSNP | rs10234329 |
| 23andMe | rs10234329 |
| SNPshot | rs10234329 |
| SNPdbe | rs10234329 |
| MSV3d | rs10234329 |
| GWAS Ctlg | rs10234329 |
| GMAF | 0.01056 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
Cystic Fibrosis mutation
| ClinVar | |
|---|---|
| Risk | rs10234329(C;C) |
| Alt | rs10234329(C;C) |
| Reference | Rs10234329(A;A) |
| Significance | Probable-non-pathogenic |
| Disease | Cystic fibrosis |
| Variation | info |
| Gene | CFTR |
| CLNDBN | Cystic fibrosis |
| Reversed | 0 |
| HGVS | NC_000007.13:g.117308205A>C |
| CLNSRC | |
| CLNACC | RCV000375001.1, |
