rs35960772
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs35960772(A;G) |
| Make rs35960772(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5226639 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35960772 |
| dbSNP (classic) | rs35960772 |
| ClinGen | rs35960772 |
| ebi | rs35960772 |
| HLI | rs35960772 |
| Exac | rs35960772 |
| Gnomad | rs35960772 |
| Varsome | rs35960772 |
| LitVar | rs35960772 |
| Map | rs35960772 |
| PheGenI | rs35960772 |
| Biobank | rs35960772 |
| 1000 genomes | rs35960772 |
| hgdp | rs35960772 |
| ensembl | rs35960772 |
| geneview | rs35960772 |
| scholar | rs35960772 |
| rs35960772 | |
| pharmgkb | rs35960772 |
| gwascentral | rs35960772 |
| openSNP | rs35960772 |
| 23andMe | rs35960772 |
| SNPshot | rs35960772 |
| SNPdbe | rs35960772 |
| MSV3d | rs35960772 |
| GWAS Ctlg | rs35960772 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35960772(G;G) |
| Alt | rs35960772(G;G) |
| Reference | Rs35960772(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN SAALE |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN SAALE |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5247869T>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000016846.2, |
[PMID 10770934] Characterization of a new electrophoretically silent hemoglobin variant. Hb saale OR alpha 2beta 2 84(EF8)Thr --> Ala.
