rs199473368
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs199473368(A;A) |
| Make rs199473368(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 70175239 |
| Gene | KCNJ2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199473368 |
| dbSNP (classic) | rs199473368 |
| ClinGen | rs199473368 |
| ebi | rs199473368 |
| HLI | rs199473368 |
| Exac | rs199473368 |
| Gnomad | rs199473368 |
| Varsome | rs199473368 |
| LitVar | rs199473368 |
| Map | rs199473368 |
| PheGenI | rs199473368 |
| Biobank | rs199473368 |
| 1000 genomes | rs199473368 |
| hgdp | rs199473368 |
| ensembl | rs199473368 |
| geneview | rs199473368 |
| scholar | rs199473368 |
| rs199473368 | |
| pharmgkb | rs199473368 |
| gwascentral | rs199473368 |
| openSNP | rs199473368 |
| 23andMe | rs199473368 |
| SNPshot | rs199473368 |
| SNPdbe | rs199473368 |
| MSV3d | rs199473368 |
| GWAS Ctlg | rs199473368 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs199473368(A;A) |
| Alt | rs199473368(A;A) |
| Reference | Rs199473368(G;G) |
| Significance | Pathogenic |
| Disease | Congenital long QT syndrome not provided |
| Variation | info |
| Gene | KCNJ2 |
| CLNDBN | Congenital long QT syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.68171380G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000058295.3, RCV000170972.3, |
