rs35477770
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs35477770(C;T) |
| Make rs35477770(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 176796 |
| Gene | HBA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35477770 |
| dbSNP (classic) | rs35477770 |
| ClinGen | rs35477770 |
| ebi | rs35477770 |
| HLI | rs35477770 |
| Exac | rs35477770 |
| Gnomad | rs35477770 |
| Varsome | rs35477770 |
| LitVar | rs35477770 |
| Map | rs35477770 |
| PheGenI | rs35477770 |
| Biobank | rs35477770 |
| 1000 genomes | rs35477770 |
| hgdp | rs35477770 |
| ensembl | rs35477770 |
| geneview | rs35477770 |
| scholar | rs35477770 |
| rs35477770 | |
| pharmgkb | rs35477770 |
| gwascentral | rs35477770 |
| openSNP | rs35477770 |
| 23andMe | rs35477770 |
| SNPshot | rs35477770 |
| SNPdbe | rs35477770 |
| MSV3d | rs35477770 |
| GWAS Ctlg | rs35477770 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35477770(A;A) rs35477770(T;T) |
| Alt | rs35477770(A;A) rs35477770(T;T) |
| Reference | Rs35477770(C;C) |
| Significance | Other |
| Disease | HEMOGLOBIN SHENYANG |
| Variation | info |
| Gene | HBA1 |
| CLNDBN | HEMOGLOBIN SHENYANG |
| Reversed | 0 |
| HGVS | NC_000016.9:g.226795C>A |
| CLNSRC | HBVAR OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000017153.2, |
[PMID 2703370] Hemoglobin Shenyang found among Uygurs in P.R. China.
[PMID 7161109] Hb Shenyang (alpha 26 (B7) Ala replaced by Glu): a new unstable variant found in China.
