rs35492035
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs35492035(C;C) |
| Make rs35492035(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5225636 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35492035 |
| dbSNP (classic) | rs35492035 |
| ClinGen | rs35492035 |
| ebi | rs35492035 |
| HLI | rs35492035 |
| Exac | rs35492035 |
| Gnomad | rs35492035 |
| Varsome | rs35492035 |
| LitVar | rs35492035 |
| Map | rs35492035 |
| PheGenI | rs35492035 |
| Biobank | rs35492035 |
| 1000 genomes | rs35492035 |
| hgdp | rs35492035 |
| ensembl | rs35492035 |
| geneview | rs35492035 |
| scholar | rs35492035 |
| rs35492035 | |
| pharmgkb | rs35492035 |
| gwascentral | rs35492035 |
| openSNP | rs35492035 |
| 23andMe | rs35492035 |
| SNPshot | rs35492035 |
| SNPdbe | rs35492035 |
| MSV3d | rs35492035 |
| GWAS Ctlg | rs35492035 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35492035(C;C) |
| Alt | rs35492035(C;C) |
| Reference | Rs35492035(G;G) |
| Significance | Other |
| Disease | HEMOGLOBIN ALTDORF |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN ALTDORF |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5246866C>G |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016248.2, |
[PMID 1261680] Hb Altdorf alpha2beta2 135 (H13) Ala leads to Pro: a new electrophoretically silent unstable haemoglobin variant from Switzerland.
