rs281865555
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs281865555(A;A) |
| Make rs281865555(A;G) |
| Make rs281865555(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 16 |
| Position | 172961 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs281865555 |
| dbSNP (classic) | rs281865555 |
| ClinGen | rs281865555 |
| ebi | rs281865555 |
| HLI | rs281865555 |
| Exac | rs281865555 |
| Gnomad | rs281865555 |
| Varsome | rs281865555 |
| LitVar | rs281865555 |
| Map | rs281865555 |
| PheGenI | rs281865555 |
| Biobank | rs281865555 |
| 1000 genomes | rs281865555 |
| hgdp | rs281865555 |
| ensembl | rs281865555 |
| geneview | rs281865555 |
| scholar | rs281865555 |
| rs281865555 | |
| pharmgkb | rs281865555 |
| gwascentral | rs281865555 |
| openSNP | rs281865555 |
| 23andMe | rs281865555 |
| SNPshot | rs281865555 |
| SNPdbe | rs281865555 |
| MSV3d | rs281865555 |
| GWAS Ctlg | rs281865555 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs281865555(G;G) |
| Alt | rs281865555(G;G) |
| Reference | rs281865555(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN I HEMOGLOBIN I (BURLINGTON) HEMOGLOBIN I (PHILADELPHIA) HEMOGLOBIN I (SKAMANIA) HEMOGLOBIN I (TEXAS) |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | HEMOGLOBIN I HEMOGLOBIN I (BURLINGTON) HEMOGLOBIN I (PHILADELPHIA) HEMOGLOBIN I (SKAMANIA) HEMOGLOBIN I (TEXAS) |
| Reversed | 0 |
| HGVS | NC_000016.9:g.222960A>G |
| CLNSRC | HBVAR OMIM Allelic Variant |
| CLNACC | RCV000016905.1, RCV000016906.1, RCV000016907.1, RCV000016908.1, RCV000016909.1, |
