rs369869993
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs369869993(C;C) |
| Make rs369869993(C;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 70206159 |
| Gene | FADD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs369869993 |
| dbSNP (classic) | rs369869993 |
| ClinGen | rs369869993 |
| ebi | rs369869993 |
| HLI | rs369869993 |
| Exac | rs369869993 |
| Gnomad | rs369869993 |
| Varsome | rs369869993 |
| LitVar | rs369869993 |
| Map | rs369869993 |
| PheGenI | rs369869993 |
| Biobank | rs369869993 |
| 1000 genomes | rs369869993 |
| hgdp | rs369869993 |
| ensembl | rs369869993 |
| geneview | rs369869993 |
| scholar | rs369869993 |
| rs369869993 | |
| pharmgkb | rs369869993 |
| gwascentral | rs369869993 |
| openSNP | rs369869993 |
| 23andMe | rs369869993 |
| SNPshot | rs369869993 |
| SNPdbe | rs369869993 |
| MSV3d | rs369869993 |
| GWAS Ctlg | rs369869993 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs369869993(C;C) |
| Alt | rs369869993(C;C) |
| Reference | Rs369869993(T;T) |
| Significance | Probable-Pathogenic |
| Disease | Infections |
| Variation | info |
| Gene | FADD |
| CLNDBN | Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations |
| Reversed | 0 |
| HGVS | NC_000011.9:g.70052265T>C |
| CLNSRC | |
| CLNACC | RCV000195419.1, |
