rs41561812
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs41561812(C;T) |
| Make rs41561812(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31271045 |
| Gene | HLA-C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41561812 |
| dbSNP (classic) | rs41561812 |
| ClinGen | rs41561812 |
| ebi | rs41561812 |
| HLI | rs41561812 |
| Exac | rs41561812 |
| Gnomad | rs41561812 |
| Varsome | rs41561812 |
| LitVar | rs41561812 |
| Map | rs41561812 |
| PheGenI | rs41561812 |
| Biobank | rs41561812 |
| 1000 genomes | rs41561812 |
| hgdp | rs41561812 |
| ensembl | rs41561812 |
| geneview | rs41561812 |
| scholar | rs41561812 |
| rs41561812 | |
| pharmgkb | rs41561812 |
| gwascentral | rs41561812 |
| openSNP | rs41561812 |
| 23andMe | rs41561812 |
| SNPshot | rs41561812 |
| SNPdbe | rs41561812 |
| MSV3d | rs41561812 |
| GWAS Ctlg | rs41561812 |
| GMAF | 0.02893 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs41561812(T;T) |
| Alt | rs41561812(T;T) |
| Reference | Rs41561812(C;C) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-C |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31238822G>A |
| CLNSRC | |
| CLNACC | |
