rs35687396
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs35687396(A;A) |
| Make rs35687396(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 5254652 |
| Gene | HBG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35687396 |
| dbSNP (classic) | rs35687396 |
| ClinGen | rs35687396 |
| ebi | rs35687396 |
| HLI | rs35687396 |
| Exac | rs35687396 |
| Gnomad | rs35687396 |
| Varsome | rs35687396 |
| LitVar | rs35687396 |
| Map | rs35687396 |
| PheGenI | rs35687396 |
| Biobank | rs35687396 |
| 1000 genomes | rs35687396 |
| hgdp | rs35687396 |
| ensembl | rs35687396 |
| geneview | rs35687396 |
| scholar | rs35687396 |
| rs35687396 | |
| pharmgkb | rs35687396 |
| gwascentral | rs35687396 |
| openSNP | rs35687396 |
| 23andMe | rs35687396 |
| SNPshot | rs35687396 |
| SNPdbe | rs35687396 |
| MSV3d | rs35687396 |
| GWAS Ctlg | rs35687396 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35687396(A;A) |
| Alt | rs35687396(A;A) |
| Reference | Rs35687396(G;G) |
| Significance | Other |
| Disease | HEMOGLOBIN F (COSENZA) |
| Variation | info |
| Gene | HBG2 |
| CLNDBN | HEMOGLOBIN F (COSENZA) |
| Reversed | 1 |
| HGVS | NC_000011.9:g.5275882C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000016132.1, |
[PMID 1726095] Hb F-Cosenza or G gamma 25(B7)Gly----Glu: a new fast-moving fetal hemoglobin variant.
