rs35548338
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs35548338(G;G) |
| Make rs35548338(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 177093 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35548338 |
| dbSNP (classic) | rs35548338 |
| ClinGen | rs35548338 |
| ebi | rs35548338 |
| HLI | rs35548338 |
| Exac | rs35548338 |
| Gnomad | rs35548338 |
| Varsome | rs35548338 |
| LitVar | rs35548338 |
| Map | rs35548338 |
| PheGenI | rs35548338 |
| Biobank | rs35548338 |
| 1000 genomes | rs35548338 |
| hgdp | rs35548338 |
| ensembl | rs35548338 |
| geneview | rs35548338 |
| scholar | rs35548338 |
| rs35548338 | |
| pharmgkb | rs35548338 |
| gwascentral | rs35548338 |
| openSNP | rs35548338 |
| 23andMe | rs35548338 |
| SNPshot | rs35548338 |
| SNPdbe | rs35548338 |
| MSV3d | rs35548338 |
| GWAS Ctlg | rs35548338 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35548338(G;G) |
| Alt | rs35548338(G;G) |
| Reference | Rs35548338(T;T) |
| Significance | Other |
| Disease | HEMOGLOBIN MOABIT |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN MOABIT |
| Reversed | 0 |
| HGVS | NC_000016.9:g.227092T>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000017117.2, |
[PMID 108887] Hemoglobin Moabit: alpha 86 (F7) Leu leads to Arg: a new unstable abnormal hemoglobin.
