rs35825479
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs35825479(C;C) |
| Make rs35825479(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5225641 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35825479 |
| dbSNP (classic) | rs35825479 |
| ClinGen | rs35825479 |
| ebi | rs35825479 |
| HLI | rs35825479 |
| Exac | rs35825479 |
| Gnomad | rs35825479 |
| Varsome | rs35825479 |
| LitVar | rs35825479 |
| Map | rs35825479 |
| PheGenI | rs35825479 |
| Biobank | rs35825479 |
| 1000 genomes | rs35825479 |
| hgdp | rs35825479 |
| ensembl | rs35825479 |
| geneview | rs35825479 |
| scholar | rs35825479 |
| rs35825479 | |
| pharmgkb | rs35825479 |
| gwascentral | rs35825479 |
| openSNP | rs35825479 |
| 23andMe | rs35825479 |
| SNPshot | rs35825479 |
| SNPdbe | rs35825479 |
| MSV3d | rs35825479 |
| GWAS Ctlg | rs35825479 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35825479(C;C) |
| Alt | rs35825479(C;C) |
| Reference | Rs35825479(T;T) |
| Significance | Other |
| Disease | HEMOGLOBIN RENERT |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN RENERT |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5246871A>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000016852.2, |
[PMID 11186258] Hb Ernz [beta123(H1)Thr-->Asn] and Hb Renert [beta133(H11)Val-->Ala]: two new neutral variants revealed by reversed phase high performance liquid chromatography analysis.
[PMID 11482884] Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
[PMID 11570728] A second case of Hb Renert [beta133(H11)Val --> Ala].
