rs34956202
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs34956202(A;A) |
| Make rs34956202(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 172959 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34956202 |
| dbSNP (classic) | rs34956202 |
| ClinGen | rs34956202 |
| ebi | rs34956202 |
| HLI | rs34956202 |
| Exac | rs34956202 |
| Gnomad | rs34956202 |
| Varsome | rs34956202 |
| LitVar | rs34956202 |
| Map | rs34956202 |
| PheGenI | rs34956202 |
| Biobank | rs34956202 |
| 1000 genomes | rs34956202 |
| hgdp | rs34956202 |
| ensembl | rs34956202 |
| geneview | rs34956202 |
| scholar | rs34956202 |
| rs34956202 | |
| pharmgkb | rs34956202 |
| gwascentral | rs34956202 |
| openSNP | rs34956202 |
| 23andMe | rs34956202 |
| SNPshot | rs34956202 |
| SNPdbe | rs34956202 |
| MSV3d | rs34956202 |
| GWAS Ctlg | rs34956202 |
| Merged from | Rs111033600 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34956202(A;A) |
| Alt | rs34956202(A;A) |
| Reference | Rs34956202(G;G) |
| Significance | Other |
| Disease | HEMOGLOBIN J (OXFORD) HEMOGLOBIN I (INTERLAKEN) HEMOGLOBIN N (COSENZA) |
| Variation | info |
| Gene | HBA2 |
| CLNDBN | HEMOGLOBIN J (OXFORD) HEMOGLOBIN I (INTERLAKEN) HEMOGLOBIN N (COSENZA) |
| Reversed | 0 |
| HGVS | NC_000016.9:g.222958G>A |
| CLNSRC | HBVAR OMIM Allelic Variant |
| CLNACC | RCV000016902.2, RCV000016903.2, RCV000016904.2, |
[PMID 10024] A new alkali-resistant hemoglobin alpha2J Oxford gammaF2 in a Sicilian baby girl with homozygous beta0 thalassemia.
[PMID 2666359] Association of Hb S [beta 6(A3)Glu----Val] and Hb I-interlaken [alpha 15(A13)Gly----Asp] in a Sicilian man; review of the occurrence of Hb I-interlaken in Sicily.
[PMID 7803274] The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.
