rs1053878
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (T;T) |
| Make rs1053878(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 133256264 |
| Gene | ABO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1053878 |
| dbSNP (classic) | rs1053878 |
| ClinGen | rs1053878 |
| ebi | rs1053878 |
| HLI | rs1053878 |
| Exac | rs1053878 |
| Gnomad | rs1053878 |
| Varsome | rs1053878 |
| LitVar | rs1053878 |
| Map | rs1053878 |
| PheGenI | rs1053878 |
| Biobank | rs1053878 |
| 1000 genomes | rs1053878 |
| hgdp | rs1053878 |
| ensembl | rs1053878 |
| geneview | rs1053878 |
| scholar | rs1053878 |
| rs1053878 | |
| pharmgkb | rs1053878 |
| gwascentral | rs1053878 |
| openSNP | rs1053878 |
| 23andMe | rs1053878 |
| SNPshot | rs1053878 |
| SNPdbe | rs1053878 |
| MSV3d | rs1053878 |
| GWAS Ctlg | rs1053878 |
| GMAF | 0.1428 |
| Max Magnitude | 0 |
Influences ABO blood group; "cis-AB phenotype" is associated with rs1053878(T)
[PMID 19169360
] Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.
| ClinVar | |
|---|---|
| Risk | Rs1053878(T;T) |
| Alt | Rs1053878(T;T) |
| Reference | Rs1053878(C;C) |
| Significance | Other |
| Disease | ABO blood group system |
| Variation | info |
| Gene | ABO |
| CLNDBN | ABO blood group system |
| Reversed | 1 |
| HGVS | NC_000009.11:g.136131651G>A |
| CLNSRC | OMIM Allelic Variant dbRBC - Blood Group Antigen Gene Mutation Database |
| CLNACC | RCV000019312.3, |
