rs35441642
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs35441642(C;C) |
| Make rs35441642(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 14934728 |
| Gene | DCLRE1C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35441642 |
| dbSNP (classic) | rs35441642 |
| ClinGen | rs35441642 |
| ebi | rs35441642 |
| HLI | rs35441642 |
| Exac | rs35441642 |
| Gnomad | rs35441642 |
| Varsome | rs35441642 |
| LitVar | rs35441642 |
| Map | rs35441642 |
| PheGenI | rs35441642 |
| Biobank | rs35441642 |
| 1000 genomes | rs35441642 |
| hgdp | rs35441642 |
| ensembl | rs35441642 |
| geneview | rs35441642 |
| scholar | rs35441642 |
| rs35441642 | |
| pharmgkb | rs35441642 |
| gwascentral | rs35441642 |
| openSNP | rs35441642 |
| 23andMe | rs35441642 |
| SNPshot | rs35441642 |
| SNPdbe | rs35441642 |
| MSV3d | rs35441642 |
| GWAS Ctlg | rs35441642 |
| GMAF | 0.1253 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35441642(C;C) |
| Alt | rs35441642(C;C) |
| Reference | Rs35441642(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | Severe combined immunodeficiency disease not specified Histiocytic medullary reticulosis |
| Variation | info |
| Gene | DCLRE1C |
| CLNDBN | Severe combined immunodeficiency disease not specified Histiocytic medullary reticulosis |
| Reversed | 0 |
| HGVS | NC_000010.10:g.14976727G>C |
| CLNSRC | ClinVar LabCorp |
| CLNACC | RCV000029657.1, RCV000244893.1, RCV000305875.1, |
