rs114970039
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs114970039(C;C) |
| Make rs114970039(C;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 198754304 |
| Gene | PTPRC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs114970039 |
| dbSNP (classic) | rs114970039 |
| ClinGen | rs114970039 |
| ebi | rs114970039 |
| HLI | rs114970039 |
| Exac | rs114970039 |
| Gnomad | rs114970039 |
| Varsome | rs114970039 |
| LitVar | rs114970039 |
| Map | rs114970039 |
| PheGenI | rs114970039 |
| Biobank | rs114970039 |
| 1000 genomes | rs114970039 |
| hgdp | rs114970039 |
| ensembl | rs114970039 |
| geneview | rs114970039 |
| scholar | rs114970039 |
| rs114970039 | |
| pharmgkb | rs114970039 |
| gwascentral | rs114970039 |
| openSNP | rs114970039 |
| 23andMe | rs114970039 |
| SNPshot | rs114970039 |
| SNPdbe | rs114970039 |
| MSV3d | rs114970039 |
| GWAS Ctlg | rs114970039 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs114970039(C;C) |
| Alt | rs114970039(C;C) |
| Reference | Rs114970039(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PTPRC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.198723433T>C |
| CLNSRC | |
| CLNACC | RCV000171165.1, |
