rs33967561
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs33967561(A;G) |
| Make rs33967561(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 176985 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs33967561 |
| dbSNP (classic) | rs33967561 |
| ClinGen | rs33967561 |
| ebi | rs33967561 |
| HLI | rs33967561 |
| Exac | rs33967561 |
| Gnomad | rs33967561 |
| Varsome | rs33967561 |
| LitVar | rs33967561 |
| Map | rs33967561 |
| PheGenI | rs33967561 |
| Biobank | rs33967561 |
| 1000 genomes | rs33967561 |
| hgdp | rs33967561 |
| ensembl | rs33967561 |
| geneview | rs33967561 |
| scholar | rs33967561 |
| rs33967561 | |
| pharmgkb | rs33967561 |
| gwascentral | rs33967561 |
| openSNP | rs33967561 |
| 23andMe | rs33967561 |
| SNPshot | rs33967561 |
| SNPdbe | rs33967561 |
| MSV3d | rs33967561 |
| GWAS Ctlg | rs33967561 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs33967561(G;G) rs33967561(T;T) |
| Alt | rs33967561(G;G) rs33967561(T;T) |
| Reference | Rs33967561(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN AICHI |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN AICHI |
| Reversed | 0 |
| HGVS | NC_000016.9:g.226984A>G |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016986.2, |
[PMID 6714429] Hemoglobin Aichi [alpha 50(CE8) His----Arg]: a new slightly unstable hemoglobin variant discovered in Japan.
[PMID 11482884] Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
