rs63749809
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs63749809(A;A) |
| Make rs63749809(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 173578 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63749809 |
| dbSNP (classic) | rs63749809 |
| ClinGen | rs63749809 |
| ebi | rs63749809 |
| HLI | rs63749809 |
| Exac | rs63749809 |
| Gnomad | rs63749809 |
| Varsome | rs63749809 |
| LitVar | rs63749809 |
| Map | rs63749809 |
| PheGenI | rs63749809 |
| Biobank | rs63749809 |
| 1000 genomes | rs63749809 |
| hgdp | rs63749809 |
| ensembl | rs63749809 |
| geneview | rs63749809 |
| scholar | rs63749809 |
| rs63749809 | |
| pharmgkb | rs63749809 |
| gwascentral | rs63749809 |
| openSNP | rs63749809 |
| 23andMe | rs63749809 |
| SNPshot | rs63749809 |
| SNPdbe | rs63749809 |
| MSV3d | rs63749809 |
| GWAS Ctlg | rs63749809 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs63749809(A;A) |
| Alt | rs63749809(A;A) |
| Reference | Rs63749809(T;T) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.223577T>A |
| CLNSRC | |
| CLNACC | |
[PMID 2347082] A new hemoglobin variant found during investigations of diabetes mellitus: Hb Pavie [alpha 135 (H18) Val----Glu].
