rs754277797
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs754277797(C;C) |
| Make rs754277797(C;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 19 |
| Position | 855770 |
| Gene | ELANE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs754277797 |
| dbSNP (classic) | rs754277797 |
| ClinGen | rs754277797 |
| ebi | rs754277797 |
| HLI | rs754277797 |
| Exac | rs754277797 |
| Gnomad | rs754277797 |
| Varsome | rs754277797 |
| LitVar | rs754277797 |
| Map | rs754277797 |
| PheGenI | rs754277797 |
| Biobank | rs754277797 |
| 1000 genomes | rs754277797 |
| hgdp | rs754277797 |
| ensembl | rs754277797 |
| geneview | rs754277797 |
| scholar | rs754277797 |
| rs754277797 | |
| pharmgkb | rs754277797 |
| gwascentral | rs754277797 |
| openSNP | rs754277797 |
| 23andMe | rs754277797 |
| SNPshot | rs754277797 |
| SNPdbe | rs754277797 |
| MSV3d | rs754277797 |
| GWAS Ctlg | rs754277797 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs754277797(C;C) |
| Alt | rs754277797(C;C) |
| Reference | Rs754277797(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ELANE |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.855770G>C |
| CLNSRC | |
| CLNACC | RCV000232592.1, |
