rs150988911
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs150988911(C;T) |
| Make rs150988911(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 150959701 |
| Gene | KCNH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150988911 |
| dbSNP (classic) | rs150988911 |
| ClinGen | rs150988911 |
| ebi | rs150988911 |
| HLI | rs150988911 |
| Exac | rs150988911 |
| Gnomad | rs150988911 |
| Varsome | rs150988911 |
| LitVar | rs150988911 |
| Map | rs150988911 |
| PheGenI | rs150988911 |
| Biobank | rs150988911 |
| 1000 genomes | rs150988911 |
| hgdp | rs150988911 |
| ensembl | rs150988911 |
| geneview | rs150988911 |
| scholar | rs150988911 |
| rs150988911 | |
| pharmgkb | rs150988911 |
| gwascentral | rs150988911 |
| openSNP | rs150988911 |
| 23andMe | rs150988911 |
| SNPshot | rs150988911 |
| SNPdbe | rs150988911 |
| MSV3d | rs150988911 |
| GWAS Ctlg | rs150988911 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs150988911(T;T) |
| Alt | rs150988911(T;T) |
| Reference | Rs150988911(C;C) |
| Significance | Untested |
| Disease | Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome |
| Variation | info |
| Gene | KCNH2 |
| CLNDBN | Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome |
| Reversed | 0 |
| HGVS | NC_000007.13:g.150656789C>T |
| CLNSRC | ClinVar University of Washington |
| CLNACC | RCV000058225.3, RCV000148529.1, RCV000226122.2, |
