rs927091191
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 10855557 |
| Gene | PIEZO2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs927091191 |
| dbSNP (classic) | rs927091191 |
| ClinGen | rs927091191 |
| ebi | rs927091191 |
| HLI | rs927091191 |
| Exac | rs927091191 |
| Gnomad | rs927091191 |
| Varsome | rs927091191 |
| LitVar | rs927091191 |
| Map | rs927091191 |
| PheGenI | rs927091191 |
| Biobank | rs927091191 |
| 1000 genomes | rs927091191 |
| hgdp | rs927091191 |
| ensembl | rs927091191 |
| geneview | rs927091191 |
| scholar | rs927091191 |
| rs927091191 | |
| pharmgkb | rs927091191 |
| gwascentral | rs927091191 |
| openSNP | rs927091191 |
| 23andMe | rs927091191 |
| SNPshot | rs927091191 |
| SNPdbe | rs927091191 |
| MSV3d | rs927091191 |
| GWAS Ctlg | rs927091191 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs927091191(C;C) |
| Alt | rs927091191(C;C) |
| Reference | Rs927091191(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000018.9:g.10855555A>C |
| CLNSRC | |
| CLNACC | RCV000489499.1, |
