rs1800582
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1800582(A;A) |
| Make rs1800582(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 144119686 |
| Gene | GYPA, LOC107986317 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1800582 |
| dbSNP (classic) | rs1800582 |
| ClinGen | rs1800582 |
| ebi | rs1800582 |
| HLI | rs1800582 |
| Exac | rs1800582 |
| Gnomad | rs1800582 |
| Varsome | rs1800582 |
| LitVar | rs1800582 |
| Map | rs1800582 |
| PheGenI | rs1800582 |
| Biobank | rs1800582 |
| 1000 genomes | rs1800582 |
| hgdp | rs1800582 |
| ensembl | rs1800582 |
| geneview | rs1800582 |
| scholar | rs1800582 |
| rs1800582 | |
| pharmgkb | rs1800582 |
| gwascentral | rs1800582 |
| openSNP | rs1800582 |
| 23andMe | rs1800582 |
| SNPshot | rs1800582 |
| SNPdbe | rs1800582 |
| MSV3d | rs1800582 |
| GWAS Ctlg | rs1800582 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1800582(A;A) |
| Alt | rs1800582(A;A) |
| Reference | Rs1800582(G;G) |
| Significance | Pathogenic |
| Disease | BLOOD GROUP ERIK |
| Variation | info |
| Gene | GYPA |
| CLNDBN | BLOOD GROUP ERIK |
| Reversed | 1 |
| HGVS | NC_000004.11:g.145040839C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019288.27, |
