rs56340844
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs56340844(C;T) |
| Make rs56340844(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 14840856 |
| Gene | ART4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56340844 |
| dbSNP (classic) | rs56340844 |
| ClinGen | rs56340844 |
| ebi | rs56340844 |
| HLI | rs56340844 |
| Exac | rs56340844 |
| Gnomad | rs56340844 |
| Varsome | rs56340844 |
| LitVar | rs56340844 |
| Map | rs56340844 |
| PheGenI | rs56340844 |
| Biobank | rs56340844 |
| 1000 genomes | rs56340844 |
| hgdp | rs56340844 |
| ensembl | rs56340844 |
| geneview | rs56340844 |
| scholar | rs56340844 |
| rs56340844 | |
| pharmgkb | rs56340844 |
| gwascentral | rs56340844 |
| openSNP | rs56340844 |
| 23andMe | rs56340844 |
| SNPshot | rs56340844 |
| SNPdbe | rs56340844 |
| MSV3d | rs56340844 |
| GWAS Ctlg | rs56340844 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs56340844(T;T) |
| Alt | rs56340844(T;T) |
| Reference | Rs56340844(C;C) |
| Significance | Other |
| Disease | Blood group |
| Variation | info |
| Gene | ART4 |
| CLNDBN | Blood group, Dombrock system |
| Reversed | 1 |
| HGVS | NC_000012.11:g.14993790G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019308.29, |
