rs1799805
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1799805(A;A) |
| Make rs1799805(A;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 100893176 |
| Gene | ACHE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799805 |
| dbSNP (classic) | rs1799805 |
| ClinGen | rs1799805 |
| ebi | rs1799805 |
| HLI | rs1799805 |
| Exac | rs1799805 |
| Gnomad | rs1799805 |
| Varsome | rs1799805 |
| LitVar | rs1799805 |
| Map | rs1799805 |
| PheGenI | rs1799805 |
| Biobank | rs1799805 |
| 1000 genomes | rs1799805 |
| hgdp | rs1799805 |
| ensembl | rs1799805 |
| geneview | rs1799805 |
| scholar | rs1799805 |
| rs1799805 | |
| pharmgkb | rs1799805 |
| gwascentral | rs1799805 |
| openSNP | rs1799805 |
| 23andMe | rs1799805 |
| SNPshot | rs1799805 |
| SNPdbe | rs1799805 |
| MSV3d | rs1799805 |
| GWAS Ctlg | rs1799805 |
| GMAF | 0.02755 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs1799805(A;A) |
| Alt | rs1799805(A;A) |
| Reference | Rs1799805(C;C) |
| Significance | Non-pathogenic |
| Disease | YT BLOOD GROUP POLYMORPHISM |
| Variation | info |
| Gene | ACHE |
| CLNDBN | YT BLOOD GROUP POLYMORPHISM |
| Reversed | 1 |
| HGVS | NC_000007.13:g.100490797G>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000020001.2, |
[PMID 21257350
] DNA-based methods in the immunohematology reference laboratory.
