rs28936699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs28936699(C;T) |
| Make rs28936699(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 201209388 |
| Gene | CASP10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28936699 |
| dbSNP (classic) | rs28936699 |
| ClinGen | rs28936699 |
| ebi | rs28936699 |
| HLI | rs28936699 |
| Exac | rs28936699 |
| Gnomad | rs28936699 |
| Varsome | rs28936699 |
| LitVar | rs28936699 |
| Map | rs28936699 |
| PheGenI | rs28936699 |
| Biobank | rs28936699 |
| 1000 genomes | rs28936699 |
| hgdp | rs28936699 |
| ensembl | rs28936699 |
| geneview | rs28936699 |
| scholar | rs28936699 |
| rs28936699 | |
| pharmgkb | rs28936699 |
| gwascentral | rs28936699 |
| openSNP | rs28936699 |
| 23andMe | rs28936699 |
| SNPshot | rs28936699 |
| SNPdbe | rs28936699 |
| MSV3d | rs28936699 |
| GWAS Ctlg | rs28936699 |
| Max Magnitude | 0 |
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
| ClinVar | |
|---|---|
| Risk | rs28936699(T;T) |
| Alt | rs28936699(T;T) |
| Reference | Rs28936699(C;C) |
| Significance | Pathogenic |
| Disease | Malignant lymphoma |
| Variation | info |
| Gene | CASP10 |
| CLNDBN | Malignant lymphoma, non-Hodgkin |
| Reversed | 0 |
| HGVS | NC_000002.11:g.202074111C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000008206.5, |
