rs115746363
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs115746363(A;A) |
| Make rs115746363(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 152312410 |
| Gene | FLG, FLG-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs115746363 |
| dbSNP (classic) | rs115746363 |
| ClinGen | rs115746363 |
| ebi | rs115746363 |
| HLI | rs115746363 |
| Exac | rs115746363 |
| Gnomad | rs115746363 |
| Varsome | rs115746363 |
| LitVar | rs115746363 |
| Map | rs115746363 |
| PheGenI | rs115746363 |
| Biobank | rs115746363 |
| 1000 genomes | rs115746363 |
| hgdp | rs115746363 |
| ensembl | rs115746363 |
| geneview | rs115746363 |
| scholar | rs115746363 |
| rs115746363 | |
| pharmgkb | rs115746363 |
| gwascentral | rs115746363 |
| openSNP | rs115746363 |
| 23andMe | rs115746363 |
| SNPshot | rs115746363 |
| SNPdbe | rs115746363 |
| MSV3d | rs115746363 |
| GWAS Ctlg | rs115746363 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs115746363(A;A) |
| Alt | rs115746363(A;A) |
| Reference | Rs115746363(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | FLG FLG-AS1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.152284886G>A |
| CLNSRC | |
| CLNACC | RCV000255117.2, |
