rs863224533
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CTT;CTT) | 0 | common in clinvar |
Make rs863224533(CTT;GTA) |
Make rs863224533(GTA;GTA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 38551525 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs863224533 |
dbSNP (classic) | rs863224533 |
ClinGen | rs863224533 |
ebi | rs863224533 |
HLI | rs863224533 |
Exac | rs863224533 |
Gnomad | rs863224533 |
Varsome | rs863224533 |
LitVar | rs863224533 |
Map | rs863224533 |
PheGenI | rs863224533 |
Biobank | rs863224533 |
1000 genomes | rs863224533 |
hgdp | rs863224533 |
ensembl | rs863224533 |
geneview | rs863224533 |
scholar | rs863224533 |
rs863224533 | |
pharmgkb | rs863224533 |
gwascentral | rs863224533 |
openSNP | rs863224533 |
23andMe | rs863224533 |
SNPshot | rs863224533 |
SNPdbe | rs863224533 |
MSV3d | rs863224533 |
GWAS Ctlg | rs863224533 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224533(GTA;GTA) |
Alt | rs863224533(GTA;GTA) |
Reference | Rs863224533(CTT;CTT) |
Significance | Pathogenic |
Disease | Brugada syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Brugada syndrome |
Reversed | 1 |
HGVS | NC_000003.11:g.38593016_38593018delAAGinsTAC |
CLNSRC | |
CLNACC | RCV000195716.1, |