rs113605136
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs113605136(C;G) |
| Make rs113605136(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 2 |
| Position | 237359089 |
| Gene | COL6A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs113605136 |
| dbSNP (classic) | rs113605136 |
| ClinGen | rs113605136 |
| ebi | rs113605136 |
| HLI | rs113605136 |
| Exac | rs113605136 |
| Gnomad | rs113605136 |
| Varsome | rs113605136 |
| LitVar | rs113605136 |
| Map | rs113605136 |
| PheGenI | rs113605136 |
| Biobank | rs113605136 |
| 1000 genomes | rs113605136 |
| hgdp | rs113605136 |
| ensembl | rs113605136 |
| geneview | rs113605136 |
| scholar | rs113605136 |
| rs113605136 | |
| pharmgkb | rs113605136 |
| gwascentral | rs113605136 |
| openSNP | rs113605136 |
| 23andMe | rs113605136 |
| SNPshot | rs113605136 |
| SNPdbe | rs113605136 |
| MSV3d | rs113605136 |
| GWAS Ctlg | rs113605136 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs113605136(A;A) rs113605136(G;G) rs113605136(T;T) |
| Alt | rs113605136(A;A) rs113605136(G;G) rs113605136(T;T) |
| Reference | Rs113605136(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COL6A3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.238267732C>T |
| CLNSRC | |
| CLNACC | RCV000397729.1, |
