rs121908735
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs121908735(C;T) |
| Make rs121908735(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 44625581 |
| Gene | ADA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121908735 |
| dbSNP (classic) | rs121908735 |
| ClinGen | rs121908735 |
| ebi | rs121908735 |
| HLI | rs121908735 |
| Exac | rs121908735 |
| Gnomad | rs121908735 |
| Varsome | rs121908735 |
| LitVar | rs121908735 |
| Map | rs121908735 |
| PheGenI | rs121908735 |
| Biobank | rs121908735 |
| 1000 genomes | rs121908735 |
| hgdp | rs121908735 |
| ensembl | rs121908735 |
| geneview | rs121908735 |
| scholar | rs121908735 |
| rs121908735 | |
| pharmgkb | rs121908735 |
| gwascentral | rs121908735 |
| openSNP | rs121908735 |
| 23andMe | rs121908735 |
| SNPshot | rs121908735 |
| SNPdbe | rs121908735 |
| MSV3d | rs121908735 |
| GWAS Ctlg | rs121908735 |
| Merged from | Rs28930971 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121908735(T;T) |
| Alt | rs121908735(T;T) |
| Reference | Rs121908735(C;C) |
| Significance | Pathogenic |
| Disease | Severe combined immunodeficiency due to ADA deficiency |
| Variation | info |
| Gene | ADA |
| CLNDBN | Severe combined immunodeficiency due to ADA deficiency |
| Reversed | 1 |
| HGVS | NC_000020.10:g.43254222G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) UniProtKB (variants) |
| CLNACC | RCV000002047.3, |
[PMID 1284479] Identification of two new missense mutations (R156C and S291L) in two ADA- SCID patients unusual for response to therapy with partial exchange transfusions.
