rs33977536
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs33977536(A;G) |
| Make rs33977536(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5226957 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs33977536 |
| dbSNP (classic) | rs33977536 |
| ClinGen | rs33977536 |
| ebi | rs33977536 |
| HLI | rs33977536 |
| Exac | rs33977536 |
| Gnomad | rs33977536 |
| Varsome | rs33977536 |
| LitVar | rs33977536 |
| Map | rs33977536 |
| PheGenI | rs33977536 |
| Biobank | rs33977536 |
| 1000 genomes | rs33977536 |
| hgdp | rs33977536 |
| ensembl | rs33977536 |
| geneview | rs33977536 |
| scholar | rs33977536 |
| rs33977536 | |
| pharmgkb | rs33977536 |
| gwascentral | rs33977536 |
| openSNP | rs33977536 |
| 23andMe | rs33977536 |
| SNPshot | rs33977536 |
| SNPdbe | rs33977536 |
| MSV3d | rs33977536 |
| GWAS Ctlg | rs33977536 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs33977536(G;G) rs33977536(T;T) |
| Alt | rs33977536(G;G) rs33977536(T;T) |
| Reference | Rs33977536(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN CONNECTICUT |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN CONNECTICUT |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5248187T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016305.3, |
[PMID 7304605] Hemoglobin connecticut (beta 21 (B3) Asp leads to Gly): a hemoglobin variant with low oxygen affinity.
[PMID 11482884] Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
