rs35187567
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs35187567(A;A) |
| Make rs35187567(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 173535 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35187567 |
| dbSNP (classic) | rs35187567 |
| ClinGen | rs35187567 |
| ebi | rs35187567 |
| HLI | rs35187567 |
| Exac | rs35187567 |
| Gnomad | rs35187567 |
| Varsome | rs35187567 |
| LitVar | rs35187567 |
| Map | rs35187567 |
| PheGenI | rs35187567 |
| Biobank | rs35187567 |
| 1000 genomes | rs35187567 |
| hgdp | rs35187567 |
| ensembl | rs35187567 |
| geneview | rs35187567 |
| scholar | rs35187567 |
| rs35187567 | |
| pharmgkb | rs35187567 |
| gwascentral | rs35187567 |
| openSNP | rs35187567 |
| 23andMe | rs35187567 |
| SNPshot | rs35187567 |
| SNPdbe | rs35187567 |
| MSV3d | rs35187567 |
| GWAS Ctlg | rs35187567 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35187567(A;A) |
| Alt | rs35187567(A;A) |
| Reference | Rs35187567(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.223534G>A |
| CLNSRC | |
| CLNACC | |
[PMID 3754245] Hb Owari [alpha 121 (H 4) Val----Met]: a new hemoglobin variant with a neutral-to-neutral amino acid substitution detected by isoelectric focusing.
