rs34876238
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs34876238(A;A) |
| Make rs34876238(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5254303 |
| Gene | HBG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34876238 |
| dbSNP (classic) | rs34876238 |
| ClinGen | rs34876238 |
| ebi | rs34876238 |
| HLI | rs34876238 |
| Exac | rs34876238 |
| Gnomad | rs34876238 |
| Varsome | rs34876238 |
| LitVar | rs34876238 |
| Map | rs34876238 |
| PheGenI | rs34876238 |
| Biobank | rs34876238 |
| 1000 genomes | rs34876238 |
| hgdp | rs34876238 |
| ensembl | rs34876238 |
| geneview | rs34876238 |
| scholar | rs34876238 |
| rs34876238 | |
| pharmgkb | rs34876238 |
| gwascentral | rs34876238 |
| openSNP | rs34876238 |
| 23andMe | rs34876238 |
| SNPshot | rs34876238 |
| SNPdbe | rs34876238 |
| MSV3d | rs34876238 |
| GWAS Ctlg | rs34876238 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34876238(A;A) rs34876238(C;C) |
| Alt | rs34876238(A;A) rs34876238(C;C) |
| Reference | Rs34876238(G;G) |
| Significance | Other |
| Disease | HEMOGLOBIN F (LA GRANGE) |
| Variation | info |
| Gene | HBG2 |
| CLNDBN | HEMOGLOBIN F (LA GRANGE) |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5275533C>T |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016107.1, |
[PMID 6206897] Hb F-La Grange or alpha 2 gamma 2 101(G3)Glu----Lys; 75Ile; 136Gly: a high oxygen affinity fetal hemoglobin variant observed in a Caucasian newborn.
