rs119473032
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs119473032(A;G) |
| Make rs119473032(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 20253576 |
| Gene | LZTS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs119473032 |
| dbSNP (classic) | rs119473032 |
| ClinGen | rs119473032 |
| ebi | rs119473032 |
| HLI | rs119473032 |
| Exac | rs119473032 |
| Gnomad | rs119473032 |
| Varsome | rs119473032 |
| LitVar | rs119473032 |
| Map | rs119473032 |
| PheGenI | rs119473032 |
| Biobank | rs119473032 |
| 1000 genomes | rs119473032 |
| hgdp | rs119473032 |
| ensembl | rs119473032 |
| geneview | rs119473032 |
| scholar | rs119473032 |
| rs119473032 | |
| pharmgkb | rs119473032 |
| gwascentral | rs119473032 |
| openSNP | rs119473032 |
| 23andMe | rs119473032 |
| SNPshot | rs119473032 |
| SNPdbe | rs119473032 |
| MSV3d | rs119473032 |
| GWAS Ctlg | rs119473032 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs119473032(G;G) |
| Alt | rs119473032(G;G) |
| Reference | Rs119473032(A;A) |
| Significance | Pathogenic |
| Disease | Esophageal squamous cell carcinoma |
| Variation | info |
| Gene | LZTS1 |
| CLNDBN | Esophageal squamous cell carcinoma, somatic |
| Reversed | 1 |
| HGVS | NC_000008.10:g.20111087T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000004468.4, |
