rs28362692
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs28362692(C;T) |
| Make rs28362692(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 30912043 |
| Gene | AQP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28362692 |
| dbSNP (classic) | rs28362692 |
| ClinGen | rs28362692 |
| ebi | rs28362692 |
| HLI | rs28362692 |
| Exac | rs28362692 |
| Gnomad | rs28362692 |
| Varsome | rs28362692 |
| LitVar | rs28362692 |
| Map | rs28362692 |
| PheGenI | rs28362692 |
| Biobank | rs28362692 |
| 1000 genomes | rs28362692 |
| hgdp | rs28362692 |
| ensembl | rs28362692 |
| geneview | rs28362692 |
| scholar | rs28362692 |
| rs28362692 | |
| pharmgkb | rs28362692 |
| gwascentral | rs28362692 |
| openSNP | rs28362692 |
| 23andMe | rs28362692 |
| SNPshot | rs28362692 |
| SNPdbe | rs28362692 |
| MSV3d | rs28362692 |
| GWAS Ctlg | rs28362692 |
| GMAF | 0.01561 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28362692(T;T) |
| Alt | rs28362692(T;T) |
| Reference | Rs28362692(C;C) |
| Significance | Non-pathogenic |
| Disease | COLTON BLOOD GROUP POLYMORPHISM |
| Variation | info |
| Gene | AQP1 |
| CLNDBN | COLTON BLOOD GROUP POLYMORPHISM |
| Reversed | 0 |
| HGVS | NC_000007.13:g.30951658C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019424.2, |
[PMID 21257350
] DNA-based methods in the immunohematology reference laboratory.
