rs185492581
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs185492581(C;C) |
Make rs185492581(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 38630327 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs185492581 |
dbSNP (classic) | rs185492581 |
ClinGen | rs185492581 |
ebi | rs185492581 |
HLI | rs185492581 |
Exac | rs185492581 |
Gnomad | rs185492581 |
Varsome | rs185492581 |
LitVar | rs185492581 |
Map | rs185492581 |
PheGenI | rs185492581 |
Biobank | rs185492581 |
1000 genomes | rs185492581 |
hgdp | rs185492581 |
ensembl | rs185492581 |
geneview | rs185492581 |
scholar | rs185492581 |
rs185492581 | |
pharmgkb | rs185492581 |
gwascentral | rs185492581 |
openSNP | rs185492581 |
23andMe | rs185492581 |
SNPshot | rs185492581 |
SNPdbe | rs185492581 |
MSV3d | rs185492581 |
GWAS Ctlg | rs185492581 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs185492581(C;C) |
Alt | rs185492581(C;C) |
Reference | Rs185492581(T;T) |
Significance | Untested |
Disease | Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.38671818T>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000058601.2, |