rs141423405
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141423405(C;T) |
Make rs141423405(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 21 |
Position | 34370707 |
Gene | KCNE2, LOC105372791 |
is a | snp |
is | mentioned by |
dbSNP | rs141423405 |
dbSNP (classic) | rs141423405 |
ClinGen | rs141423405 |
ebi | rs141423405 |
HLI | rs141423405 |
Exac | rs141423405 |
Gnomad | rs141423405 |
Varsome | rs141423405 |
LitVar | rs141423405 |
Map | rs141423405 |
PheGenI | rs141423405 |
Biobank | rs141423405 |
1000 genomes | rs141423405 |
hgdp | rs141423405 |
ensembl | rs141423405 |
geneview | rs141423405 |
scholar | rs141423405 |
rs141423405 | |
pharmgkb | rs141423405 |
gwascentral | rs141423405 |
openSNP | rs141423405 |
23andMe | rs141423405 |
SNPshot | rs141423405 |
SNPdbe | rs141423405 |
MSV3d | rs141423405 |
GWAS Ctlg | rs141423405 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141423405(T;T) |
Alt | rs141423405(T;T) |
Reference | Rs141423405(C;C) |
Significance | Untested |
Disease | Congenital long QT syndrome Long QT syndrome not specified |
Variation | info |
Gene | KCNE2 |
CLNDBN | Congenital long QT syndrome Long QT syndrome not specified |
Reversed | 0 |
HGVS | NC_000021.8:g.35743006C>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000058367.3, RCV000148522.1, RCV000170957.4, |