rs33936967
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs33936967(G;G) |
| Make rs33936967(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5226647 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs33936967 |
| dbSNP (classic) | rs33936967 |
| ClinGen | rs33936967 |
| ebi | rs33936967 |
| HLI | rs33936967 |
| Exac | rs33936967 |
| Gnomad | rs33936967 |
| Varsome | rs33936967 |
| LitVar | rs33936967 |
| Map | rs33936967 |
| PheGenI | rs33936967 |
| Biobank | rs33936967 |
| 1000 genomes | rs33936967 |
| hgdp | rs33936967 |
| ensembl | rs33936967 |
| geneview | rs33936967 |
| scholar | rs33936967 |
| rs33936967 | |
| pharmgkb | rs33936967 |
| gwascentral | rs33936967 |
| openSNP | rs33936967 |
| 23andMe | rs33936967 |
| SNPshot | rs33936967 |
| SNPdbe | rs33936967 |
| MSV3d | rs33936967 |
| GWAS Ctlg | rs33936967 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs33936967(A;A) rs33936967(G;G) |
| Alt | rs33936967(A;A) rs33936967(G;G) |
| Reference | Rs33936967(T;T) |
| Significance | Other |
| Disease | HEMOGLOBIN BAYLOR HEMOGLOBIN LA ROCHE-SUR-YON |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN BAYLOR HEMOGLOBIN LA ROCHE-SUR-YON |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5247877A>C; NC_000011.9:g.5247877A>T |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016259.3, RCV000016837.2, |
[PMID 1540659] Structure of the EF corner favors deamidation of asparaginyl residues in hemoglobin: the example of Hb La Roche-sur-Yon [beta 81 (EF5) Leu----His].
