rs119477056
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs119477056(C;T) |
| Make rs119477056(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 111585362 |
| Gene | CD96 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs119477056 |
| dbSNP (classic) | rs119477056 |
| ClinGen | rs119477056 |
| ebi | rs119477056 |
| HLI | rs119477056 |
| Exac | rs119477056 |
| Gnomad | rs119477056 |
| Varsome | rs119477056 |
| LitVar | rs119477056 |
| Map | rs119477056 |
| PheGenI | rs119477056 |
| Biobank | rs119477056 |
| 1000 genomes | rs119477056 |
| hgdp | rs119477056 |
| ensembl | rs119477056 |
| geneview | rs119477056 |
| scholar | rs119477056 |
| rs119477056 | |
| pharmgkb | rs119477056 |
| gwascentral | rs119477056 |
| openSNP | rs119477056 |
| 23andMe | rs119477056 |
| SNPshot | rs119477056 |
| SNPdbe | rs119477056 |
| MSV3d | rs119477056 |
| GWAS Ctlg | rs119477056 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs119477056(A;A) rs119477056(T;T) |
| Alt | rs119477056(A;A) rs119477056(T;T) |
| Reference | Rs119477056(C;C) |
| Significance | Pathogenic |
| Disease | C syndrome |
| Variation | info |
| Gene | CD96 |
| CLNDBN | C syndrome |
| Reversed | 0 |
| HGVS | NC_000003.11:g.111304209C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000004903.2, |
