rs761877421
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (TC;TC) | 0 | common in clinvar |
| Make rs761877421(-;-) |
| Make rs761877421(-;TC) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 152313588 |
| Gene | FLG, FLG-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761877421 |
| dbSNP (classic) | rs761877421 |
| ClinGen | rs761877421 |
| ebi | rs761877421 |
| HLI | rs761877421 |
| Exac | rs761877421 |
| Gnomad | rs761877421 |
| Varsome | rs761877421 |
| LitVar | rs761877421 |
| Map | rs761877421 |
| PheGenI | rs761877421 |
| Biobank | rs761877421 |
| 1000 genomes | rs761877421 |
| hgdp | rs761877421 |
| ensembl | rs761877421 |
| geneview | rs761877421 |
| scholar | rs761877421 |
| rs761877421 | |
| pharmgkb | rs761877421 |
| gwascentral | rs761877421 |
| openSNP | rs761877421 |
| 23andMe | rs761877421 |
| SNPshot | rs761877421 |
| SNPdbe | rs761877421 |
| MSV3d | rs761877421 |
| GWAS Ctlg | rs761877421 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs761877421(-;-) |
| Alt | rs761877421(-;-) |
| Reference | Rs761877421(TC;TC) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FLG FLG-AS1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.152286064_152286065delTC |
| CLNSRC | |
| CLNACC | RCV000490026.1, |
