rs267606892
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs267606892(C;C) |
| Make rs267606892(C;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | MT |
| Position | 10563 |
| Gene | ND4L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267606892 |
| dbSNP (classic) | rs267606892 |
| ClinGen | rs267606892 |
| ebi | rs267606892 |
| HLI | rs267606892 |
| Exac | rs267606892 |
| Gnomad | rs267606892 |
| Varsome | rs267606892 |
| LitVar | rs267606892 |
| Map | rs267606892 |
| PheGenI | rs267606892 |
| Biobank | rs267606892 |
| 1000 genomes | rs267606892 |
| hgdp | rs267606892 |
| ensembl | rs267606892 |
| geneview | rs267606892 |
| scholar | rs267606892 |
| rs267606892 | |
| pharmgkb | rs267606892 |
| gwascentral | rs267606892 |
| openSNP | rs267606892 |
| 23andMe | rs267606892 |
| SNPshot | rs267606892 |
| SNPdbe | rs267606892 |
| MSV3d | rs267606892 |
| GWAS Ctlg | rs267606892 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs267606892(C;C) |
| Alt | rs267606892(C;C) |
| Reference | Rs267606892(T;T) |
| Significance | Pathogenic |
| Disease | Familial colorectal cancer |
| Variation | info |
| Gene | ND4L |
| CLNDBN | Familial colorectal cancer |
| Reversed | 0 |
| HGVS | NC_012920.1:m.10563T>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000010352.2, |
