rs147445322
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs147445322(A;A) |
| Make rs147445322(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 2847803 |
| Gene | KCNQ1, KCNQ1-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs147445322 |
| dbSNP (classic) | rs147445322 |
| ClinGen | rs147445322 |
| ebi | rs147445322 |
| HLI | rs147445322 |
| Exac | rs147445322 |
| Gnomad | rs147445322 |
| Varsome | rs147445322 |
| LitVar | rs147445322 |
| Map | rs147445322 |
| PheGenI | rs147445322 |
| Biobank | rs147445322 |
| 1000 genomes | rs147445322 |
| hgdp | rs147445322 |
| ensembl | rs147445322 |
| geneview | rs147445322 |
| scholar | rs147445322 |
| rs147445322 | |
| pharmgkb | rs147445322 |
| gwascentral | rs147445322 |
| openSNP | rs147445322 |
| 23andMe | rs147445322 |
| SNPshot | rs147445322 |
| SNPdbe | rs147445322 |
| MSV3d | rs147445322 |
| GWAS Ctlg | rs147445322 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs147445322(A;A) rs147445322(T;T) |
| Alt | rs147445322(A;A) rs147445322(T;T) |
| Reference | Rs147445322(G;G) |
| Significance | Other |
| Disease | Congenital long QT syndrome Long QT syndrome not specified |
| Variation | info |
| Gene | KCNQ1-AS1 KCNQ1 |
| CLNDBN | Congenital long QT syndrome Long QT syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000011.9:g.2869033G>A; NC_000011.9:g.2869033G>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000057643.3, RCV000148559.3, RCV000182235.3, RCV000057644.3, |
