rs1040238147
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 189050640 |
| Gene | COL5A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1040238147 |
| dbSNP (classic) | rs1040238147 |
| ClinGen | rs1040238147 |
| ebi | rs1040238147 |
| HLI | rs1040238147 |
| Exac | rs1040238147 |
| Gnomad | rs1040238147 |
| Varsome | rs1040238147 |
| LitVar | rs1040238147 |
| Map | rs1040238147 |
| PheGenI | rs1040238147 |
| Biobank | rs1040238147 |
| 1000 genomes | rs1040238147 |
| hgdp | rs1040238147 |
| ensembl | rs1040238147 |
| geneview | rs1040238147 |
| scholar | rs1040238147 |
| rs1040238147 | |
| pharmgkb | rs1040238147 |
| gwascentral | rs1040238147 |
| openSNP | rs1040238147 |
| 23andMe | rs1040238147 |
| SNPshot | rs1040238147 |
| SNPdbe | rs1040238147 |
| MSV3d | rs1040238147 |
| GWAS Ctlg | rs1040238147 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1040238147(T;T) |
| Alt | rs1040238147(T;T) |
| Reference | Rs1040238147(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COL5A2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.189915366C>T |
| CLNSRC | |
| CLNACC | RCV000483758.1, |
