rs33957766
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs33957766(A;T) |
| Make rs33957766(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 173551 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs33957766 |
| dbSNP (classic) | rs33957766 |
| ClinGen | rs33957766 |
| ebi | rs33957766 |
| HLI | rs33957766 |
| Exac | rs33957766 |
| Gnomad | rs33957766 |
| Varsome | rs33957766 |
| LitVar | rs33957766 |
| Map | rs33957766 |
| PheGenI | rs33957766 |
| Biobank | rs33957766 |
| 1000 genomes | rs33957766 |
| hgdp | rs33957766 |
| ensembl | rs33957766 |
| geneview | rs33957766 |
| scholar | rs33957766 |
| rs33957766 | |
| pharmgkb | rs33957766 |
| gwascentral | rs33957766 |
| openSNP | rs33957766 |
| 23andMe | rs33957766 |
| SNPshot | rs33957766 |
| SNPdbe | rs33957766 |
| MSV3d | rs33957766 |
| GWAS Ctlg | rs33957766 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs33957766(G;G) rs33957766(T;T) |
| Alt | rs33957766(G;G) rs33957766(T;T) |
| Reference | Rs33957766(A;A) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.223550A>G; NC_000016.9:g.223550A>T |
| CLNSRC | |
| CLNACC | |
[PMID 2079432] Hb Fukutomi [alpha 126(H9)Asp----Val]: a new hemoglobin variant with high oxygen affinity.
