rs199544087
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs199544087(A;A) |
| Make rs199544087(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 4 |
| Position | 1805761 |
| Gene | FGFR3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199544087 |
| dbSNP (classic) | rs199544087 |
| ClinGen | rs199544087 |
| ebi | rs199544087 |
| HLI | rs199544087 |
| Exac | rs199544087 |
| Gnomad | rs199544087 |
| Varsome | rs199544087 |
| LitVar | rs199544087 |
| Map | rs199544087 |
| PheGenI | rs199544087 |
| Biobank | rs199544087 |
| 1000 genomes | rs199544087 |
| hgdp | rs199544087 |
| ensembl | rs199544087 |
| geneview | rs199544087 |
| scholar | rs199544087 |
| rs199544087 | |
| pharmgkb | rs199544087 |
| gwascentral | rs199544087 |
| openSNP | rs199544087 |
| 23andMe | rs199544087 |
| SNPshot | rs199544087 |
| SNPdbe | rs199544087 |
| MSV3d | rs199544087 |
| GWAS Ctlg | rs199544087 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs199544087(A;A) rs199544087(T;T) |
| Alt | rs199544087(A;A) rs199544087(T;T) |
| Reference | Rs199544087(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Myeloproliferative disorder |
| Variation | info |
| Gene | FGFR3 |
| CLNDBN | Myeloproliferative disorder |
| Reversed | 0 |
| HGVS | NC_000004.11:g.1807488G>A |
| CLNSRC | |
| CLNACC | RCV000418578.1, |
