rs33973589
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs33973589(C;G) |
| Make rs33973589(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5225673 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs33973589 |
| dbSNP (classic) | rs33973589 |
| ClinGen | rs33973589 |
| ebi | rs33973589 |
| HLI | rs33973589 |
| Exac | rs33973589 |
| Gnomad | rs33973589 |
| Varsome | rs33973589 |
| LitVar | rs33973589 |
| Map | rs33973589 |
| PheGenI | rs33973589 |
| Biobank | rs33973589 |
| 1000 genomes | rs33973589 |
| hgdp | rs33973589 |
| ensembl | rs33973589 |
| geneview | rs33973589 |
| scholar | rs33973589 |
| rs33973589 | |
| pharmgkb | rs33973589 |
| gwascentral | rs33973589 |
| openSNP | rs33973589 |
| 23andMe | rs33973589 |
| SNPshot | rs33973589 |
| SNPdbe | rs33973589 |
| MSV3d | rs33973589 |
| GWAS Ctlg | rs33973589 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs33973589(A;A) rs33973589(G;G) rs33973589(T;T) |
| Alt | rs33973589(A;A) rs33973589(G;G) rs33973589(T;T) |
| Reference | Rs33973589(C;C) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBB |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5246903G>C; NC_000011.9:g.5246903G>T |
| CLNSRC | |
| CLNACC | |
[PMID 10870883] Two new variants with the same substitution at position beta122: Hb Bushey [beta122(GH5)Phe-->Leu] and Hb Casablanca [beta65(E9)lys-->Met; beta122(GH5)Phe-->Leu].
