rs35693898
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs35693898(C;C) |
| Make rs35693898(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5226635 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35693898 |
| dbSNP (classic) | rs35693898 |
| ClinGen | rs35693898 |
| ebi | rs35693898 |
| HLI | rs35693898 |
| Exac | rs35693898 |
| Gnomad | rs35693898 |
| Varsome | rs35693898 |
| LitVar | rs35693898 |
| Map | rs35693898 |
| PheGenI | rs35693898 |
| Biobank | rs35693898 |
| 1000 genomes | rs35693898 |
| hgdp | rs35693898 |
| ensembl | rs35693898 |
| geneview | rs35693898 |
| scholar | rs35693898 |
| rs35693898 | |
| pharmgkb | rs35693898 |
| gwascentral | rs35693898 |
| openSNP | rs35693898 |
| 23andMe | rs35693898 |
| SNPshot | rs35693898 |
| SNPdbe | rs35693898 |
| MSV3d | rs35693898 |
| GWAS Ctlg | rs35693898 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35693898(C;C) |
| Alt | rs35693898(C;C) |
| Reference | Rs35693898(T;T) |
| Significance | Pathogenic |
| Disease | Hemoglobinopathy |
| Variation | info |
| Gene | HBB |
| CLNDBN | Hemoglobinopathy |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5247865A>G |
| CLNSRC | HBVAR OMIM Allelic Variant |
| CLNACC | RCV000016279.5, |
[PMID 4205171] A new unstable haemoglobin: Hb Buenos Aires, beta 85 (F1) Phe leads to Ser.
