rs35977759
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs35977759(A;G) |
| Make rs35977759(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5249564 |
| Gene | HBG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35977759 |
| dbSNP (classic) | rs35977759 |
| ClinGen | rs35977759 |
| ebi | rs35977759 |
| HLI | rs35977759 |
| Exac | rs35977759 |
| Gnomad | rs35977759 |
| Varsome | rs35977759 |
| LitVar | rs35977759 |
| Map | rs35977759 |
| PheGenI | rs35977759 |
| Biobank | rs35977759 |
| 1000 genomes | rs35977759 |
| hgdp | rs35977759 |
| ensembl | rs35977759 |
| geneview | rs35977759 |
| scholar | rs35977759 |
| rs35977759 | |
| pharmgkb | rs35977759 |
| gwascentral | rs35977759 |
| openSNP | rs35977759 |
| 23andMe | rs35977759 |
| SNPshot | rs35977759 |
| SNPdbe | rs35977759 |
| MSV3d | rs35977759 |
| GWAS Ctlg | rs35977759 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35977759(G;G) |
| Alt | rs35977759(G;G) |
| Reference | Rs35977759(A;A) |
| Significance | Other |
| Disease | HEMOGLOBIN F (BONAIRE) |
| Variation | info |
| Gene | HBG1 |
| CLNDBN | HEMOGLOBIN F (BONAIRE) |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5270794T>C |
| CLNSRC | HBVAR OMIM Allelic Variant |
| CLNACC | RCV000016148.1, |
[PMID 6186637] Hb F-Bonaire-Ga or alpha 2 A gamma 2 39(C5) Gln replaced by Arg, characterized by high pressure liquid chromatographic and microsequencing procedures.
