rs397515458
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397515458(C;T) |
Make rs397515458(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 123503899 |
Gene | TRDN |
is a | snp |
is | mentioned by |
dbSNP | rs397515458 |
dbSNP (classic) | rs397515458 |
ClinGen | rs397515458 |
ebi | rs397515458 |
HLI | rs397515458 |
Exac | rs397515458 |
Gnomad | rs397515458 |
Varsome | rs397515458 |
LitVar | rs397515458 |
Map | rs397515458 |
PheGenI | rs397515458 |
Biobank | rs397515458 |
1000 genomes | rs397515458 |
hgdp | rs397515458 |
ensembl | rs397515458 |
geneview | rs397515458 |
scholar | rs397515458 |
rs397515458 | |
pharmgkb | rs397515458 |
gwascentral | rs397515458 |
openSNP | rs397515458 |
23andMe | rs397515458 |
SNPshot | rs397515458 |
SNPdbe | rs397515458 |
MSV3d | rs397515458 |
GWAS Ctlg | rs397515458 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515458(T;T) |
Alt | rs397515458(T;T) |
Reference | Rs397515458(C;C) |
Significance | Pathogenic |
Disease | Ventricular tachycardia not provided |
Variation | info |
Gene | TRDN |
CLNDBN | Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.123825044G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000056260.3, RCV000484797.1, |