rs760446904
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs760446904(C;T) |
| Make rs760446904(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 237361132 |
| Gene | COL6A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs760446904 |
| dbSNP (classic) | rs760446904 |
| ClinGen | rs760446904 |
| ebi | rs760446904 |
| HLI | rs760446904 |
| Exac | rs760446904 |
| Gnomad | rs760446904 |
| Varsome | rs760446904 |
| LitVar | rs760446904 |
| Map | rs760446904 |
| PheGenI | rs760446904 |
| Biobank | rs760446904 |
| 1000 genomes | rs760446904 |
| hgdp | rs760446904 |
| ensembl | rs760446904 |
| geneview | rs760446904 |
| scholar | rs760446904 |
| rs760446904 | |
| pharmgkb | rs760446904 |
| gwascentral | rs760446904 |
| openSNP | rs760446904 |
| 23andMe | rs760446904 |
| SNPshot | rs760446904 |
| SNPdbe | rs760446904 |
| MSV3d | rs760446904 |
| GWAS Ctlg | rs760446904 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs760446904(T;T) |
| Alt | rs760446904(T;T) |
| Reference | Rs760446904(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | COL6A3 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.238269775C>T |
| CLNSRC | |
| CLNACC | RCV000274706.1, RCV000494333.1, |
