rs184830847
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs184830847(A;A) |
| Make rs184830847(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 14 |
| Position | 95103721 |
| Gene | DICER1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs184830847 |
| dbSNP (classic) | rs184830847 |
| ClinGen | rs184830847 |
| ebi | rs184830847 |
| HLI | rs184830847 |
| Exac | rs184830847 |
| Gnomad | rs184830847 |
| Varsome | rs184830847 |
| LitVar | rs184830847 |
| Map | rs184830847 |
| PheGenI | rs184830847 |
| Biobank | rs184830847 |
| 1000 genomes | rs184830847 |
| hgdp | rs184830847 |
| ensembl | rs184830847 |
| geneview | rs184830847 |
| scholar | rs184830847 |
| rs184830847 | |
| pharmgkb | rs184830847 |
| gwascentral | rs184830847 |
| openSNP | rs184830847 |
| 23andMe | rs184830847 |
| SNPshot | rs184830847 |
| SNPdbe | rs184830847 |
| MSV3d | rs184830847 |
| GWAS Ctlg | rs184830847 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs184830847(A;A) |
| Alt | rs184830847(A;A) |
| Reference | Rs184830847(G;G) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | DICER1 |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000014.8:g.95570058G>C |
| CLNSRC | |
| CLNACC | RCV000494286.1, |
