rs28933384
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (G;G) | 0 | common in complete genomics |
| Make rs28933384(C;T) |
| Make rs28933384(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 34449615 |
| Gene | KCNE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28933384 |
| dbSNP (classic) | rs28933384 |
| ClinGen | rs28933384 |
| ebi | rs28933384 |
| HLI | rs28933384 |
| Exac | rs28933384 |
| Gnomad | rs28933384 |
| Varsome | rs28933384 |
| LitVar | rs28933384 |
| Map | rs28933384 |
| PheGenI | rs28933384 |
| Biobank | rs28933384 |
| 1000 genomes | rs28933384 |
| hgdp | rs28933384 |
| ensembl | rs28933384 |
| geneview | rs28933384 |
| scholar | rs28933384 |
| rs28933384 | |
| pharmgkb | rs28933384 |
| gwascentral | rs28933384 |
| openSNP | rs28933384 |
| 23andMe | rs28933384 |
| SNPshot | rs28933384 |
| SNPdbe | rs28933384 |
| MSV3d | rs28933384 |
| GWAS Ctlg | rs28933384 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28933384(T;T) |
| Alt | rs28933384(T;T) |
| Reference | Rs28933384(C;C) |
| Significance | Pathogenic |
| Disease | Jervell and Lange-Nielsen syndrome 2 Congenital long QT syndrome |
| Variation | info |
| Gene | KCNE1B KCNE1 |
| CLNDBN | Jervell and Lange-Nielsen syndrome 2 Congenital long QT syndrome |
| Reversed | 1 |
| HGVS | NC_000021.8:g.35821913G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000014418.25, RCV000119076.2, |
[PMID 19214780
] In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).
