rs34188626
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs34188626(C;C) |
| Make rs34188626(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5225646 |
| Gene | HBB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34188626 |
| dbSNP (classic) | rs34188626 |
| ClinGen | rs34188626 |
| ebi | rs34188626 |
| HLI | rs34188626 |
| Exac | rs34188626 |
| Gnomad | rs34188626 |
| Varsome | rs34188626 |
| LitVar | rs34188626 |
| Map | rs34188626 |
| PheGenI | rs34188626 |
| Biobank | rs34188626 |
| 1000 genomes | rs34188626 |
| hgdp | rs34188626 |
| ensembl | rs34188626 |
| geneview | rs34188626 |
| scholar | rs34188626 |
| rs34188626 | |
| pharmgkb | rs34188626 |
| gwascentral | rs34188626 |
| openSNP | rs34188626 |
| 23andMe | rs34188626 |
| SNPshot | rs34188626 |
| SNPdbe | rs34188626 |
| MSV3d | rs34188626 |
| GWAS Ctlg | rs34188626 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34188626(C;C) |
| Alt | rs34188626(C;C) |
| Reference | Rs34188626(G;G) |
| Significance | Other |
| Disease | HEMOGLOBIN SILVER SPRINGS |
| Variation | info |
| Gene | HBB |
| CLNDBN | HEMOGLOBIN SILVER SPRINGS |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5246876C>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000016830.2, |
[PMID 9494046] Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-Americans.
